EP3554266A1 - Multi-drug antibody drug conjugates - Google Patents
Multi-drug antibody drug conjugatesInfo
- Publication number
- EP3554266A1 EP3554266A1 EP17879927.6A EP17879927A EP3554266A1 EP 3554266 A1 EP3554266 A1 EP 3554266A1 EP 17879927 A EP17879927 A EP 17879927A EP 3554266 A1 EP3554266 A1 EP 3554266A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- group
- antibody
- drug
- attached
- unit
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
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- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
- A61K47/6889—Conjugates wherein the antibody being the modifying agent and wherein the linker, binder or spacer confers particular properties to the conjugates, e.g. peptidic enzyme-labile linkers or acid-labile linkers, providing for an acid-labile immuno conjugate wherein the drug may be released from its antibody conjugated part in an acidic, e.g. tumoural or environment
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2878—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the NGF-receptor/TNF-receptor superfamily, e.g. CD27, CD30, CD40, CD95
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/30—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2803—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
Definitions
- ADCs Antibody-drug conjugates combine the tumor targeting specificity of monoclonal antibodies with the potent cell-killing activity of cytotoxic warheads.
- ADCETRISTM brentuximab vedotin
- KADCYLATM in HER2-positive metastatic breast cancer.
- Most of these new methodologies have focused on addressing some of the shortcomings of existing clinical molecules, such as heterogeneous drug loading, limited drug-linker stability, and warheads with activities that are restricted to a subset of cancer types.
- ADCs To enable improved ADCs, much notable advancement has been made in the field. These include site-specific drug-linker conjugation strategies that enable homogeneous loading, drug-linker attachment modalities with improved stability, potent new payloads, and linker strategies that utilize alternative release mechanisms.
- That technology which is applicable for other targeting agents, demonstrates the first use of orthogonal thiol protecting groups for preparing ADCs which is not dependent on an engineered antibody.
- auristatin drug-linkers also referred to as auristatin Linking Assembly Units, include mc-MMAF (1), mc-vc-MMAF (2), and mc-vc-MMAE (3).
- the released drug from the mc-vc- MMAE drug linker, monomethyl auristatin E (MMAE) is cell-permeable and exhibits bystander activity, or the killing of neighboring antigen-negative cancer cells.
- MMAE is also a substrate for multiple drug resistant (MDR) exporters and thus has diminished activity on cells with high MDR expression.
- MDR multiple drug resistant
- MMAF and cys-mc-MMAF, released from mc-vc- MMAF and mc-MMAF ADCs respectively are not susceptible to drug export and retain activity on MDR(+) cells but are minimally cell-permeable. Thus, they do not exhibit bystander activity and have little activity on antigen-negative tumor cells. Combining the features of both types of drugs could provide complementary activities on cancers, yielding ADCs with enhanced cytotoxicity profiles.
- One such method utilized pyridazine-dione re- bridging of reduced native antibody disulfides followed by dual-Click functionalization to construct a largely homogeneous product, but this method was only used to create a fluorophore- drug antibody conjugate and consumed two conjugatable sites on the antibody, thus reducing potential total drug loading.
- MD-ADCs multi-drug antibody drug conjugates
- LA Linking Assembly Unit
- each of the up to eight covalently attached Linking Assembly Units are attached to a thiol produced by reduction of interchain disulfide linkages in the antibody and/or each of the covalently attached LA Units is attached to a thiol from an engineered cysteine residue
- each of the covalently attached Linking Assembly Units has from two to four drug moieties, also referred to as Drug Units, attached thereto in which two of the Drug Units are different and an optional Partitioning Agent (Y).
- Y Partitioning Agent
- MD-ADCs are provided in formulae (I), (II), (III) and (IV), as well as formulae (I*), (II*), (III*), and (IV*).
- Linking Assembly Units that are useful in the preparation of the MD-ADCs, which are embodied by formulae (la), (Ila), (Ilia) (IVa), and (XHIa).
- Protected Linking Assembly Units (useful in preparing the Linking Assembly Units and the MD-ADCs), which are embodied by formulae (lb), (lib), (Illb), (IVb), and (XHIb) below.
- antibody conjugates having 1 to 8 orthogonally protected Linking Assembly Units.
- compositions, and methods for treating diseases, using the MD-ADCs described are provided herein as pharmaceutical compositions, and methods for treating diseases, using the MD-ADCs described.
- FIG. 1A and IB show the total ion chromatogram (TIC) and UV chromatogram (280 nm) after reverse-phase separation of light and heavy chain antibodies after conjugation (A) and after deprotection (B).
- the deconvoluted mass spectra for the main light and heavy chain species are shown to the right of the chromatograph, with the expected and observed masses shown. Note that multiple heavy chain mass species are present due to heterogeneity in the N-linked glycan. Only the GO glycoform mass is noted for the heavy chain.
- LC light chain
- HC heavy chain.
- FIG. 2A and 2B shows the deconvoluted light chain mass of cAClO-mc-Cys after acetamidomethyl (Acm) deprotection and subsequent N-ethyl maleimide (NEM) addition, which either included prior treatment with QMP resin (A) or did not (B). Addition of NEM to the liberated thiol was only observed in (A).
- FIG. 3 shows that mercury-mediated Acm deprotection does not affect antibody interchain disulfide integrity.
- Maleimidocaproyl-Cys(Acm) was conjugated to cAC10(S239C) at 2 carriers per antibody. This conjugate had all interchain disulfide bonds intact.
- the conjugate was subjected to mercury-mediated Acm deprotection conditions and subsequent N-ethyl maleimide (NEM) conjugation (ca. 20 molar equivalents). Shown are the deconvoluted light and heavy chain mass spectra following reverse-phase separation of light and heavy chains. This analysis demonstrates that only a single NEM molecule was added to the heavy chain and no modification of the light chain occurred.
- NEM N-ethyl maleimide
- FIG. 4 shows a reaction schematic that includes the conditions for sequential unmasking of Cys(SiPr) and Cys(Acm) residues on carrier 4 and the resulting site-specific drug- linker conjugation.
- Each conjugate was analyzed by reverse-phase UPLC-MS. Shown below each intermediate is the UV chromatogram following reverse-phase separation, and the de- convoluted light chain mass. Each step proceeded with near quantitative conversion, yielding largely a single light and heavy chain species. The de-convoluted heavy chain mass for each conjugate is provided in FIG. 6.
- FIG. 5 shows the total ion chromatogram (TIC) and UV chromatogram (280 nm) after reverse-phase separation of light and heavy chain.
- TIC total ion chromatogram
- UV chromatogram 280 nm
- FIG. 6 shows the deconvoluted heavy chain mass of drug-carrier conjugate cAClO-4 before (top) and after -SiPr removal and conjugation of 1 (middle), and -Acm removal and conjugation of 3.
- FIG. 7 shows SEC characterization of the MD-ADC cAC 10-1-3 prepared using drug carrier 4. The conjugate was 98 % monomelic (6.77 min).
- FIG. 8 shows saturation binding of cACIO antibody, cAC10-4-(3-l) ADC, or non- binding IgGt isotype control on CD30(+) L540cy cells.
- the calculated KD values for cACIO naked antibody and cAC10-4-(3-l) were 0.35 nM and 0.50 nM, respectively.
- FIG. 9 A and 9B show in vitro activity of cAC 10 ADCs against a panel of cell lines. All three ADCs utilize the multiplexing drug carrier 4.
- the second Cys residue was capped with 8 copies of N-ethyl maleimide. Activity is reported as IC50 in ng/mL of ADC.
- panel A cells were treated with ADCs for 96 hours, and cell viability was determined using Cell TiterGlo (Promega), while in panel B cell viability was determined using the Bright- Glo luciferase assay system (Promega).
- FfL Hodgkin lymphoma
- ALCL anaplastic large cell lymphoma.
- FIG. 10 shows an isotype control ADC (IgGl-4-(l-3)) was inactive on CD30(+) L540cy cells whereas cAC10-4-(l-3) was highly active.
- FIG. 11 shows Dual-drug ADC activity on MDR(+) DEL-BVR xenograft model in vivo. Each MD-ADC was prepared using drug carrier 4. For single-drug conjugates, the second Cys residue was capped with 8 copies of N-ethyl maleimide.
- FIG. 12 shows MD-ADC activity on an in vivo xenograft model with heterogeneous CD30 expression.
- the xenograft model consisted of a 1 :1 mixture of Karpas 299 (CD30+) and Karpas 35R (CD30-) cells.
- Each MD-ADC was prepared using drug carrier 4.
- the second Cys residue was capped with 8 copies of N-ethyl maleimide.
- FIG. 13 shows that the multi-drug ADC comprising Comp. Aa and Comp. Ab limits the outgrowth of ADC-resistant cells as compared to ADCs with single-drug loading (just Comp. Aa or just Comp. Ab) in the chronic treatment assay. This experiment was performed with JHH- 7 cells.
- FIG. 14 shows that the multi-drug ADC comprising Comp. Aa and Comp. Ab limits the outgrowth of ADC-resistant cells as compared to ADCs with single-drug loading (just Comp. Aa or just Comp Ab) or untreated cells in the colony forming assay. This experiment was performed with JHH-7 cells.
- FIG. 15 shows that the multi-drug ADC comprising Comp. Aa and MMAE limits the outgrowth of ADC-resistant cells as compared to ADCs with single-drug loading (just Comp. Aa or just MMAE) or untreated cells in the colony forming assay. This experiment was performed with MCF-7 cells.
- FIG. 14 shows that the multi-drug ADC comprising Comp. Aa and Comp. Ab limits the outgrowth of ADC-resistant cells as compared to ADCs with single-drug loading (just Comp. Aa or just Comp Ab) or untreated cells in the colony forming assay. This experiment was performed with JHH-7 cells.
- FIG. 15 shows that the multi-drug
- 16A-B show analytical data for preparing a drug carrier bearing 3 cysteines for 16 + 8 drug loading.
- A UV chromatogram (280 nm) after reverse-phase separation of light and heavy chain of the 24-load MD ADC. Note that a single light and heavy chain peak are present. The peak eluting at 1.44 min is fully loaded light chain (LC). The peak eluting at 1.91 min is fully loaded heavy chain (HC);
- B Deconvoluted light chain mass of a 24-load (16 + 8) MD ADC using drug carrier 3 on cACIO antibody The observed m/z corresponds to a fully conjugated light chain bearing carrier 3, and 3 total drug units (split 2 + 1).
- FIG. 17A-E show analytical data for preparing a dual loaded L49- Linking Assembly UnitAb (8)-Comp. Aj(8)-Comp. Ak (8) without a PEG group.
- A UV chromatogram (280 nm) after reverse-phase separation of light and heavy chain of the MD ADC. The peak eluting at 1.07 min is fully loaded LC. The peak eluting at 1.62 min is fully loaded HC. The peak eluting at 1.46 min is under-loaded for the second conjugated drug (2 drugs per HC instead of 3);
- B UV chromatogram
- MD-ADCs multi-drug antibody drug conjugates
- Preparation of the MD-ADCs utilizes an orthogonal protection strategy for constructing the Linking Assembly Unit, which in an MD-ADC conjugates the dual drugs to the targeting antibody, in an approach that enables both high drug loading in a defined assembly, yet is flexible to allow for different stoichiometries of the drugs (ratios of Drug 1 to Drug 2).
- each Drug Linker Assembly Unit or orthogonally protected intermediate thereof, to the MD-ADC.
- the orthogonal protection is either in the Linking Assembly Unit of an Antibody-Linker Assembly Unit intermediate, prior to covalent attachment of one or both of D 1 and D 2 or a Multiple Drug Linker (MD-Linker) compound, which is used in the preparation of the MD-ADC, in which one or both of the D 1 and D 2 are covalently attached.
- MD-Linker Multiple Drug Linker
- a Drug Linking Assembly Unit is a Linking Assembly Unit where Drug Units (D 1 and/or D 2 ) are covalently attached to the linking Assembly Unit
- an orthogonally protected Linking Assembly Unit is a Linking Assembly Unit where Protecting Groups (P 1 and P 2 ) are covalently attached to a Linking Assembly Unit.
- this application refers to a Linking Assembly Unit without specifying Drug or orthogonally protected. Based on the context of the paragraph, it will be apparent to the skilled reader if the reference to Linking Assembly Unit refers to the Drug Linking Assembly Unit, the orthogonally protected Linking Assembly Unit, both, or an intermediate thereof.
- the MD-ADCs provided herein further provide the advantage that multiple drugs can be successfully targeted to a particular binding site through conjugation to the same antibody which overcomes the difficulties associated with, for example, the delivery of an ADC1/ADC2 combination in which ADCl has one of the two different drugs to be delivered and ADC2 has the other drug.
- ADC1/ADC2 combination in which ADCl has one of the two different drugs to be delivered and ADC2 has the other drug.
- ADCl and ADC2 (1) the conjugates compete for antigen binding, leading to large differences in drug delivery and activity on cells, particularly those with lower antigen copy number, or (2) are cleared at different rates leading to pharmacodynamic variability for exposures of the two drugs to the same targeted cells.
- antibody as used herein is used in the broadest sense and specifically covers intact monoclonal antibodies, polyclonal antibodies, monospecific antibodies, multispecific antibodies (e.g., bispecific antibodies), and antibody fragments that exhibit the desired biological activity provided that the antibody fragment have the requisite number of attachment sites for a drug-linker.
- the native form of an antibody is a tetramer and consists of two identical pairs of immunoglobulin chains, each pair having one light chain and one heavy chain.
- the light and heavy chain variable regions are together primarily responsible for binding to an antigen.
- the light chain and heavy chain variable domains consist of a framework region interrupted by three hypervariable regions, also called “complementarity determining regions" or "CDRs.”
- the constant regions may be recognized by and interact with the immune system, (see, e.g., Janeway et al, 2001, Immuno. Biology, 5th Ed., Garland Publishing, New York).
- An antibody includes any isotype (e.g., IgG, IgE, IgM, IgD, and IgA), or subclass (e.g., IgGl, IgG2, IgG3, IgG4, IgAl and IgA2) thereof.
- the antibody is derivable from any suitable species.
- the antibody is of human or murine origin, and in other aspects an antibody is a human, humanized or chimeric antibody.
- the term "monoclonal antibody” as used herein refers to an antibody obtained from a population of substantially homogeneous antibodies, i.e., the individual antibodies comprising the population are identical except for possible naturally-occurring mutations that may be present in minor amounts. Monoclonal antibodies are highly specific, being directed against a single antigenic site. The modifier “monoclonal” indicates the character of the antibody as being obtained from a substantially homogeneous population of antibodies, and is not to be construed as requiring production of the antibody by any particular method.
- an "intact antibody” is one which comprises an antigen-binding variable region as well as a light chain constant domain (CL) and heavy chain constant domains, CHI , CH2, CH3 and CH4, as appropriate for the antibody class.
- the constant domains are either native sequence constant domains (e.g., human native sequence constant domains) or amino acid sequence variant thereof.
- an "antibody fragment” comprises a portion of an intact antibody comprising the antigen-binding or variable region thereof.
- the antibody fragment must have the requisite number of sites for attachment to a drug-linker, referred herein as a Drug Linking Assembly Unit. That is, antibody fragments of the present disclosure typically include all 8 cysteine residues that form the 4 disulfide bonds found in a natural antibody such that when fully reduced each cysteine residue is available for drug loading via the Linking Assembly Unit.
- An "antigen" is an entity to which an antibody is capable of specifically binding.
- the terms “specific binding” and “specifically binds” mean that the antibody or antibody fragment thereof will bind, in a selective manner, with its corresponding target antigen and not with a multitude of other antigens.
- the antibody or antibody derivative binds with an affinity of at least about lxlO "7 M, and more typically 10 "8 M to 10 "9 M, 10 "10 M, 10 "11 M, or 10 "12 M and binds to the predetermined antigen with an affinity that is at least two-fold greater than its affinity for binding to a non-specific antigen (e.g., BSA, casein) other than the predetermined antigen or a closely-related antigen.
- a non-specific antigen e.g., BSA, casein
- inhibitor means to reduce by a measurable amount, or to prevent entirely.
- terapéuticaally effective amount refers to an amount of a Conjugate effective to treat a disease or disorder in a mammal.
- the therapeutically effective amount of the conjugate provides one or more of the following biological effects:
- the term “substantial” or “substantially” refers to a majority, i.e. >50% of a population, of a mixture or a sample, typically more than 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97 %, 98%, or 99% of a population.
- intracellularly cleaved and intracellular cleavage refer to a metabolic process or reaction inside a cell on an MD-ADC, whereby the covalent attachment, between the Drug Unit (D 1 or D 2 ) and the Linking Assembly Unit (LA) or the antibody (Ab) is broken, resulting in free drug being dissociated from the MD-ADC, including degradant products thereof, inside the cell. The moieties resulting from that dissociation are thus intracellular metabolites.
- cytotoxic activity refers to a cell-killing effect of a drug or MD-ADC or an intracellular metabolite of a MD-ADC. Cytotoxic activity is typically expressed by an IC50 value, which is the concentration (molar or mass) per unit volume at which half the cells survive exposure to a cytotoxic agent.
- cytostatic activity refers to an anti-proliferative effect other than cell killing of a cytostatic agent, or a MD-ADC having a cytostatic agent as its Drug Unit or an intracellular metabolite thereof wherein the metabolite is a cytostatic agent.
- cytotoxic agent refers to a substance that has cytotoxic activity and causes destruction of cells.
- the term is intended to include chemotherapeutic agents, and toxins such as small molecule toxins or enzymatically active toxins of bacterial, fungal, plant or animal origin, including synthetic analogs and derivatives thereof.
- cytostatic agent refers to a substance that has cytostatic activity e.g., inhibits a function of cells responsible for or that contributes to cell growth or multiplication. Cytostatic agents include inhibitors such as protein inhibitors, e.g., enzyme inhibitors. [0048]
- cancer and “cancerous” refer to or describe the physiological condition or disorder in mammals that is typically characterized by unregulated cell growth. A “tumor” comprises one or more cancerous cells.
- An "autoimmune disease” herein is a disease or disorder arising from and directed against an individual's own tissues or proteins.
- "Patient” as used herein refers to a subject to which an MD-ADC is administered.
- a “patient” include, but are not limited to, a human, rat, mouse, guinea pig, non- human primate, pig, goat, cow, horse, dog, cat, bird and fowl.
- a patient is a rat, mouse, dog, non-human primate or human.
- the patient is a human in need of an effective amount of an MD-ADC.
- beneficial or desired clinical results include, but are not limited to, alleviation of symptoms, diminishment of extent of disease, stabilized (i.e., not worsening) state of disease, delay or slowing of disease progression, amelioration or palliation of the disease state, and remission (whether partial or total), whether detectable or undetectable.
- Treatment in some aspects also means prolonging survival as compared to expected survival if not receiving treatment. Those in need of treatment include those already with the condition or disorder and in some aspects further include those prone to have the condition or disorder.
- treating includes any or all of: inhibiting growth of tumor cells, cancer cells, or of a tumor; inhibiting replication of tumor cells or cancer cells, lessening of overall tumor burden or decreasing the number of cancerous cells, and ameliorating one or more symptoms associated with the disease.
- salt refers to organic or inorganic salts of a compound (e.g., a Drug, a Linking Assembly Unit, or a MD-ADC).
- the compound contains at least one amino group, and accordingly acid addition salts can be formed with the amino group.
- Exemplary salts include, but are not limited to, sulfate, trifluoroacetate, citrate, acetate, oxalate, chloride, bromide, iodide, nitrate, bisulfate, phosphate, acid phosphate, isonicotinate, lactate, salicylate, acid citrate, tartrate, oleate, tannate, pantothenate, bitartrate, ascorbate, succinate, maleate, gentisinate, fumarate, gluconate, glucuronate, saccharate, formate, benzoate, glutamate, methanesulfonate, ethanesulfonate, benzenesulfonate, ?-toluenesulfonate, and pamoate (i.
- a salt may involve the inclusion of another molecule such as an acetate ion, a succinate ion or other counterion.
- the counterion may be any organic or inorganic moiety that stabilizes the charge on the parent compound.
- a salt has one or more than one charged atom in its structure. In instances where there are multiple charged atoms as part of the salt multiple counter ions are sometimes present. Hence, a salt can have one or more charged atoms and/or one or more counterions.
- “pharmaceutically acceptable salt” is one that is suitable for administration to a subject as described herein and in some aspects includes salts as described by P. H. Stahl and C. G.
- alkyl by itself or as part of another term refers to an unsubstituted straight chain or branched, saturated hydrocarbon having the indicated number of carbon atoms (e.g., "-Ci-Cs alkyl” or “-d-do " alkyl refer to an alkyl group having from 1 to 8 or 1 to 10 carbon atoms, respectively). When the number of carbon atoms is not indicated, the alkyl group has from 1 to 8 carbon atoms.
- Representative straight chain "-d-C 8 alkyl” groups include, but are not limited to, -methyl, -ethyl, -n-propyl, -n-butyl, -n-pentyl, -n-hexyl, -n-heptyl and -n-octyl; while branched -d-C 8 alkyls include, but are not limited to, -isopropyl, -sec-butyl, -isobutyl, -tert-butyl, -isopentyl, and -2-methylbutyl; the term "alkenyl" by itself or as part of another term refers to an unsaturated -C 2 -C 8 alkyls include, but are not limited to, -vinyl, -allyl, -
- alkynyl by itself or as part of another term refers to an unsaturated -C 2 -C 8 alkyls having one or more triple bonds, for example, -acetylenyl, -propynyl, -1-butynyl, -2-butynyl, -1-pentynyl, - 2-pentynyl and -3-methyl-l butynyl.
- alkylene refers to a substituted or unsubstituted saturated or unsaturated branched or straight chain or cyclic hydrocarbon radical of the stated number of carbon atoms, typically 1-10 carbon atoms, and having two monovalent radical centers derived by the removal of two hydrogen atoms from the same or two different carbon atoms of a parent alkane.
- Typical alkylene radicals include, but are not limited to: methylene (-CH 2 -), 1,2-ethylene (-CH 2 CH 2 -), 1,3-propylene (-CH 2 CH 2 CH 2 -), 1,4- butylene (-CH 2 CH 2 CH 2 CH 2 -), and the like.
- an alkylene is a branched or straight chain hydrocarbon (i.e., it is not a cyclic hydrocarbon). In other aspects, the alkylene is a saturated alkylene that typically is not a cyclic hydrocarbon.
- aryl by itself or as part of another term, means a substituted or unsubstituted monovalent carbocyclic aromatic hydrocarbon radical of 6-20 carbon (preferably 6-14 carbon) atoms derived by the removal of one hydrogen atom from a single carbon atom of a parent aromatic ring system. Some aryl groups are represented in the exemplary structures as "Ar".
- Typical aryl groups include, but are not limited to, radicals derived from benzene, substituted benzene, naphthalene, anthracene, biphenyl, and the like.
- An exemplary aryl group is a phenyl group.
- an "arylene,” by itself or as part of another term, is an aryl group as defined above wherein one of the aryl group's hydrogen atoms is replaced with a bond (i.e., it is divalent) and can be in the ortho, meta, or para orientations as shown in the following structures, with phenyl as the exemplary group:
- a "C 3 -C 8 heterocycle,” by itself or as part of another term, refers to a monovalent substituted or unsubstituted aromatic or non-aromatic monocyclic or bicyclic ring system having from 3 to 8 carbon atoms (also referred to as ring members) and one to four heteroatom ring members independently selected from N, O, P or S, and derived by removal of one hydrogen atom from a ring atom of a parent ring system.
- One or more N, C or S atoms in the heterocycle can be oxidized.
- the ring that includes the heteroatom can be aromatic or nonaromatic.
- heterocycle is attached to its pendant group at any heteroatom or carbon atom that results in a stable structure.
- Representative examples of a C 3 -C 8 heterocycle include, but are not limited to, pyrrolidinyl, azetidinyl, piperidinyl, morpholinyl, tetrahydrofuranyl, tetrahydropyranyl, benzofuranyl, benzothiophene, indolyl, benzopyrazolyl, pyrrolyl, thiophenyl (thiophene), furanyl, thiazolyl, imidazolyl, pyrazolyl, pyrimidinyl, pyridinyl, pyrazinyl, pyridazinyl, isothiazolyl, and isoxazolyl.
- C 3 -C 8 heterocyclo refers to a C 3 -C 8 heterocycle group defined above wherein one of the heterocycle group's hydrogen atoms is replaced with a bond (i.e., it is divalent).
- the heterocyclo is a heterocycle group defined above wherein one or two of the heterocycle group's hydrogen atoms is replaced with a bond (i.e., the heterocyclo can be divalent or trivalent).
- C 3 -C 8 carbocycle by itself or as part of another term, is a 3-, 4-, 5-, 6-, 7- or 8-membered monovalent, substituted or unsubstituted, saturated or unsaturated non-aromatic monocyclic or bicyclic carbocyclic ring derived by the removal of one hydrogen atom from a ring atom of a parent ring system.
- Representative -C 3 -C 8 carbocycles include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentadienyl, cyclohexyl, cyclohexenyl, 1,3-cyclohexadienyl, 1,4-cyclohexadienyl, cycloheptyl, 1,3- cycloheptadienyl, 1,3,5-cycloheptatrienyl, cyclooctyl, and cyclooctadienyl.
- a "C 3 -C 8 carbocyclo" refers to a C 3 -C 8 carbocycle group defined above wherein another of the carbocycle groups' hydrogen atoms is replaced with a bond (i.e., it is divalent).
- the carbocyclo is a carbocycle group defined above wherein one or two of the carbocycle group's hydrogen atoms is replaced with a bond (i.e., the carbocyclo can be divalent or trivalent).
- heteroalkyl by itself or in combination with another term, means, unless otherwise stated, a stable straight or branched chain hydrocarbon, or combinations thereof, fully saturated or containing from 1 to 3 degrees of unsaturation, consisting of the stated number of carbon atoms and from one to ten, preferably one to three, heteroatoms selected from the group consisting of O, N, Si and S, and wherein the nitrogen and sulfur atoms may optionally be oxidized and the nitrogen heteroatom may optionally be quaternized.
- the heteroatom(s) O, N and S may be placed at any interior position of the heteroalkyl group or at the position at which the alkyl group is attached to the remainder of the molecule.
- the heteroatom Si may be placed at any position of the heteroalkyl group, including the position at which the alkyl group is attached to the remainder of the molecule.
- a Q to C 4 heteroalkyl or heteroalkylene has 1 to 4 carbon atoms and 1 or 2 heteroatoms and a d to C 3 heteroalkyl or heteroalkylene has 1 to 3 carbon atoms and 1 or 2 heteroatoms.
- a heteroalkyl or heteroalkylene is saturated.
- heteroalkylene by itself or as part of another substituent means a divalent group derived from heteroalkyl (as discussed above), as exemplified by -CH 2 -CH 2 -S-CH 2 -CH 2 - and -CH 2 -S-CH 2 -CH 2 -NH-CH 2 -.
- heteroalkylene groups heteroatoms can also occupy either or both of the chain termini.
- alkylene and heteroalkylene linking groups no orientation of the linking group is implied.
- an Attachment Group or Tethering Group comprises a heteroalkylene
- heteroalkylene is a heteroalkyl group defined above wherein one or two of the heteroalkyl group's hydrogen atoms is replaced with a bond (i.e., the heteroalkylene can be divalent or trivalent).
- Substituted alkyl and “substituted aryl” mean alkyl and aryl, respectively, in which one or more hydrogen atoms are each independently replaced with a substituent.
- Typical substituents include, but are not limited to, -X, -O " , -OR, -SR, -S " , -NR 2 , -NR3,
- Alkylene, carbocycle, carbocyclo, arylene, heteroalkyl, heteroalkylene, heterocycle, and heterocyclo groups as described above are unsubstituted or similarly substituted.
- substituents for "alkyl” and “alkylene” include -X, -0 ⁇ -OR, -SR, -S "
- free drug refers to a biologically active drug moiety that is not covalently attached either directly or indirectly to any other portion of the MD-ADC or to a degradant product of a MD-ADC. Accordingly, free drug either refers to the drug prior to conjugation or as it exists immediately upon cleavage from a Drug Linking Assembly Unit of a MD-ADC via a release mechanism, which may be provided by the Optional Linking Groups in the MD-ADC, or to subsequent intracellular conversion or metabolism. In some aspects, the free drug will have the form H-D, which in some aspects exist as a charged moiety.
- the free drug is a pharmacologically active species capable of exerting the desired biological effect.
- the pharamacologically active species is the parent drug and in other aspects includes a component or vestige of a Linking Assembly Unit that has not undergone subsequent intracellular metabolism.
- Partitioning Agent is a structural unit that masks the hydrophobicity of particular Drug Units or Linking Assembly Units.
- a partitioning Agent is a structural unit that masks the hydrophobicity of particular Drug Units or Linking Assembly Units.
- Partitioning Agent increases the hydrophilic character of a Drug Linking Assembly Unit. In other aspects, Partitioning Agents improve the pharmacokinetic properties of the Linking Assembly Units or MD-ADC 's to which they are attached.
- self-stabilizing linker assembly refers to substituted succinimide) with a basic functional group proximal to a succinimide capable of catalyzing the hydrolysis of a carbonyl-nitrogen bond of the substituted succinimide.
- the hydrolysis of a substituted succinimide by the basic functional group forms a self-stabilized linker. Further details of the self-stabilizing linker assembly are described in WO 2013/173337. In some aspects the self-stabilizing linker assembly is MDPr, which has the structure disclosed herein.
- engineered cysteine residue or "eCys residue” refers to a cysteine amino acid or a derivative thereof that is incorporated into an antibody.
- One or more eCys residues can be incorporated into an antibody, and typically, the eCys residues are incorporated in either the heavy chain or the light chain of an antibody.
- incorporation of an eCys residue into an antibody is performed by mutagenizing a nucleic acid sequence of a parent antibody to encode for one or more amino acid residues with a cysteine or a derivative thereof.
- Suitable mutations include replacement of a desired residue in the light or heavy chain of an antibody with a cysteine or a derivative thereof, incorporation of an additional cysteine or a derivative thereof at a desired location in the light or heavy chain of an antibody, as well as adding an additional cysteine or a derivative thereof to the N- and/or C-terminus of a desired heavy or light chain of an amino acid.
- Derivatives of cysteine (Cys) include, but are not limited to beta-2-Cys, beta-3-Cys, homocysteine, and N-methyl cysteine.
- MD-ADCs multi-drug antibody drug conjugates
- DLA Drug Linking Assembly Unit
- PPA orthogonally Protected Linking Assembly Units
- Y Partitioning Agent
- MD-ADCs multi-drug antibody drug conjugates
- two different Drug Units are covalently attached to antibodies for simultaneous targeted delivery of two different drugs in a therapeutic protocol.
- the two drugs are attached in an integer ratio, and in some aspects are in a 1:1 ratio, a 2:1 ratio or a 3:1 ratio on each Linking Assembly Unit.
- an antibody of an MD-ADC has from 1 to 8 Linking Assembly Units attached thereto which in some aspects is connected to two different Drug Units for a total of 2 to 32 Drug Units (D J +D 2 ) per antibody, more typically 2 to 10 for a total of 2 to 20 Drug Units.
- a total drug loading of 16 (D 1 to D 2 Drug Unit in 1 : 1 ratio) is achieved by completely reducing the antibody so that each of the four inter-chain disulfide linkages is cleaved to produce eight thiols used for attachment of Linking Assembly Units or orthogonally protected Linking Assembly Units.
- the Linking Assembly Units and orthogonally protected Linking Assembly Units are further designed to have optional attachment sites that connect to Partitioning Agents (e.g., PEG groups).
- the Partitioning Agents are attachable to a variety of sites on the Linking Assembly Unit or orthogonally protected Linking Assembly Units as will be discussed more completely below.
- the Linking Assembly Units are attached to an antibody at one or more engineered cysteine (eCys) residues.
- eCys residue is a cysteine amino acid or a derivative thereof that is incorporated into the heavy chain or light chain of an antibody. It is understood that one or more eCys residues can be incorporated into a single antibody.
- Antibodies comprising eCys residues are prepared by mutagenizing a nucleic acid sequence of a parent antibody to encode for one or more amino acid residues with a cysteine. A person of skill in the art can determine suitable positions for incorporation of the eCys residues, and further information can be found in U.S. Pat. No. 9,000,130, the contents of which is incorporated herein for all purposes.
- the Drug Linking Assembly Units i.e. Linking Assembly Units with attached Drug Units
- Linking Assembly Units with Protecting Groups are typically constructed prior to attachment to an antibody - and are discussed below in the context of an assembled Linking Assembly Unit with attached Drug Units.
- Linking Assembly Units with Protecting Groups may be attached to antibodies, where the Protecting Groups are removed and Drug Units are added after addition to the antibody.
- a Linking Assembly (LA) Unit is characterized by the following features: (1) an antibody Tethering Group which facilitates attachment of LA to the antibody thiols; (2)
- a Drug Linking Assembly (DLA) Unit has Drug Units attached.
- the DLA Unit is characterized by the structure of Formula (la):
- T is a Tethering Group that provides covalent attachment of LA to antibody thiols produced by reduction of an antibody's interchain disulfide linkages
- Q 1 is a first Attachment Group that provides covalent attachment to a first Drug Unit (D 1 );
- Q 2 is a second Attachment Group that provides covalent attachment to a second Drug Unit (D 2 ); each X is an Attachment Group Linker that provides a connection, or spacing between two
- D 1 is a first Drug Unit
- D 2 is a second Drug Unit
- L 1 is an Optional Linking Group joining D 1 to Q 1 ;
- L 2 is an Optional Linking Group joining D 2 to Q 2 ;
- subscripts m 1 and m 2 are each independently 0 or 1;
- Y is a Partitioning Agent
- n 0 or 1.
- the DLA Unit is characterized by the structure of Formula (Ila):
- T is a Tethering Group provides covalent attachment of LA to antibody thiols produced by
- each Q 1 is a first Attachment Group that provides covalent attachment of a first Drug Unit (D 1 );
- Q 2 is a second Attachment Group that provides covalent attachment of a second Drug Unit (D 2 );
- X is an Attachment Group Linker
- D 1 is a first Drug Unit
- D 2 is a second Drug Unit
- L 1 is an Optional Linking Group joining D 1 to Q 1 ;
- L 2 is an Optional Linking Group joining D 2 to Q 2 ;
- subscripts m 1 and m 2 are each independently 0 or 1;
- Y is a Partitioning Agent
- n 0 or 1.
- the DLA Unit is characterized by the structure of Formula (Ilia):
- T is a Tethering Group that provides covalent attachment of LA to antibody thiols produced by reduction of an antibody's interchain disulfide linkages
- each Q 1 is an independently selected first Attachment Group that provides covalent attachment of an independently selected first Drug Unit (D 1 );
- Q 2 is a second Attachment Group that provides covalent attachment of a second Drug Unit (D 2 );
- X 1 and X 2 are each an Attachment Group Linker
- D 1 is a first Drug Unit
- D 2 is a second Drug Unit
- L 1 is an Optional Linking Group joining D 1 to Q 1 ;
- L 2 is an Optional Linking Group joining D 2 to Q 2 ;
- subscripts m 1 and m 2 are each independently 0 or 1;
- Y is a Partitioning Agent
- n 0 or 1.
- the DLA Unit is characterized by the structure of the Formula (IVa)
- T is a Tethering Group that provides covalent attachment of LA to antibody thiols produced by reduction of an antibody's interchain disulfide linkages
- each Q 1 is an independently selected first Attachment Group that provides covalent attachment of an independently selected first Drug Unit (D 1 );
- Q 2 is a second Attachment Group that provides covalent attachment of a second Drug Unit (D 2 );
- X 1 and X 2 are each an independently selected Attachment Group Linker;
- D 1 is a first Drug Unit
- D 2 is a second Drug Unit
- L 1 is an Optional Linking Group joining D 1 to Q 1 ;
- L 2 is an Optional Linking Group joining D 2 to Q 2 ;
- subscripts m 1 and m 2 are each independently 0 or 1;
- Y is a Partitioning Agent
- n 0 or 1.
- a Tethering Group (T) refers to the portion of a Linking Assembly Unit that provides covalent and uniform attachment to antibody thiols.
- the structural requirements of (T) for the purpose include a functional group that provies covalent attachment to an antibody thiol, and a functional group that provides covalent attachment to a first Attachment Group (Q 1 ).
- Tethering Group will in some embodiments have a site providing covalent attachment to a Partitioning Agent (Y).
- Y Partitioning Agent
- Tethering Groups A number of functional groups suitable as Tethering Groups have been described in the literature and include those functional groups designed for attachment to a thiol moiety present in an antibody. Those functional groups include maleimido moieties (e.g., maleimidocaproyl and self-stabilizing moieties such as mDPR, see WO 2013/173337).
- Tethering Groups prior to covalent attachment to an antibody thiol, within the scope of the present disclosure include, groups of Formulas (V) and (VI)
- LG is a leaving group
- the wavy line to the right is an Attachment Group (Q 1 and Q 2 )
- R 19 is as defined below.
- the maleimide of Formula (V) is capable of reacting with a thiol of an antibody, and with reference to Formula VI, the thiol of an antibody will covalently attach to the carbon bearing LG via nucleophilic attack to displace the leaving group (LG).
- Suitable leaving groups are well known to one of skill in the art and include halogen, tosylate, and mesylate.
- a Tethering Group prior to covalent attachment to an antibody thiol, has formula (VII)
- R 23 is a di-, or tri-peptide.
- the amino acids in the peptide unit of R 23 are independently selected from valine, alanine, glycine, leucine, and citrulline.
- substituted maleimide shown in Formula (V) and Formula (VII) will in some embodiments exist in hydrolyzed form(s) after attachment to an antibody thiol. That is, in exemplary embodiments, the resulting substituted succinimide is in hydrolyzed form(s) as shown below:
- the R 19 substituents of Formulas (V) and (VI) are optionally substituted.
- the R 19 substituent of formula (V) is substituted by a Basic Unit, e.g (CH 2 )xNH 2 ,(CH 2 )xNHR a , and (CH 2 ) x NR a 2 , wherein subscript x is an integer ranging from 1-4 and each R a is an independently selected Ci-C 6 alkyl, or two R a groups are combined with the nitrogen to which they are attached to form an azetidinyl, pyrrolidinyl or piperidinyl group.
- the Tethering Group (T) prior to covalent attachment to an antibody thiol, is selected from the group consisting of
- the Tethering Group (T), prior to attachment to an antibody thiol is, for example, a maleimido-containing linker moiety that is cleavable by a protease.
- exemplary T Units cleavable by a protease for use with the MD-ADCs described herein include the following structures wherein, S is the sulfur atom of an antibody thiol, the wavy line to the right is an Attachment Group Linker, and the wavy line to the left is the antibody:
- Attachment Groups useful in the LA Units described herein are those groups having functional groups that can be protected Orthogonally' - protected to allow for selective de- protection when the attachment of a Drug Unit (D 1 or D 2 ) is being carried out.
- Protecting Groups (P 1 and P 2 ) of the present disclosure are discussed in greater detail in a later section.
- the Attachment Groups are natural or non-natural amino acids comprising a reactive functional group for attachment of a Protecting Group, a Drug Unit, or an Optional Linking Group.
- Those include amino acids with functional groups such as thiol, amine, hydroxyl, carboxylic acid, or amide such as, cysteine, serine, threonine, tyrosine, lysine, citrulline, arginine, aspartate, glutamate, asparagine, and glutamine.
- Those functional groups are capable of reacting with a suitable corresponding group on the Protecting Group, Drug Unit, or Optional Linking Group.
- the Attachment Groups (Q 1 and Q 2 ) are independently selected from amino acids such as cysteine, serine, threonine, lysine, citrulline, and arginine. In some embodiments the Attachment Groups (Q 1 and Q 2 ) are independently selected from the group consisting of cysteine, serine, and lysine. In some embodiments, the Attachment Groups (Q 1 and Q 2 ) are cysteine.
- the Attachment Groups (Q 1 and Q 2 ) are independently selected from cysteine (Cys) derivatives such as Cys (StBu), H-Cys(Acm)-OH, H-Cys(Trt)-OH, H- Cys(StBu)-OH, H-Cys(Bzl)-OH, H-Cys(S-Et)-OH, H-Cys(S0 3 H)-OH, H-Cys(aminoethyl)-OH, H-Cys(carbamoyl)-OH, H-Cys(S-phenyl)-OH, H-Cys(Boc)-OH, and H-Cys(hydroxyethyl)-OH.
- cysteine (Cys) derivatives such as Cys (StBu), H-Cys(Acm)-OH, H-Cys(Trt)-OH, H- Cys(StBu)-OH, H-C
- the Attachment Groups (Q 1 and Q 2 ) are independently selected from cysteine (Cys) derivatives such as Cys(Stmp), Cys(Mmt), Thiaproline, Cys(Dpm), Cys(Thp), Cys(4-MeOBzl), Cys(Npys), Cys(Cys).
- the Attachment Groups (Q 1 and Q 2 ) are independently selected from cysteine (Cys) derivatives such as beta-2-Cys, beta-3-Cys, homocysteine, and N-methyl cysteine.
- suitable covalent attachments between the Attachment Group and adjacent groups or linkages include disulfides, thioethers, peptides, hydrazine, ester, or carbamate bonds.
- Attachment Groups do not have to include an amino acid residue. So long as the Attachment Group comprises a functional group that is capable of being protected / deprotected Orthogonally' and are further comprised of chemical groups that are capable of covalent attachment to the Attachment Group Linker and/or the optional Linking unit, said Attachment Group are also suitable components of a Linking Assembly Unit.
- Attachment Group Linkers (X, X 1 , X 2 , and X s ) [0096] To provide suitable spacing between Attachment Groups, Linking Assembly Units provided herein include, in some embodiments, Attachment Group Linkers (X, X 1 and X 2 ). Those Attachment Group Linkers are typically groups that, in addition to providing spacing between the Attachment Groups (Q 1 and Q 2 ), will result in benign components when the MC- ADC composition is metabolized in vivo. Typical Attachment Group Linkers are, for example, glycine, alanine, ⁇ -alanine, and di-peptide or tri-peptides.
- amino acids While a variety of amino acids are useful in this context, preferred amino acids are those having side chains that do not require protection/de-protection steps during construction of the LA.
- suitable amino acids that do not require protection/de-protecting steps during construction of the LA include glycine, alanine, ⁇ -alanine, valine, leucine, phenylalanine, and proline.
- the Attachment Group Linker is an amino acid, the amino position on each amino acid may be substituted or unsubstituted.
- an Attachments Group Linker (X, X 1 , or X 2 ) is a di-peptide wherein each peptide is independently selected from the group consisting glycine, alanine, ⁇ - alanine, valine, leucine, phenylalanine, and proline.
- an Attachments Group Linker (X, X 1 , or X 2 ) is a tri-peptide wherein each peptide is independently selected from the group consisting glycine, alanine, ⁇ - alanine, valine, leucine, phenylalanine, and proline.
- an Attachment Group Linker is branched. That is Attachment Groups (Q 1 and Q 2 ) are attached to a single Attachment Group Linker (X B ). In such embodiments,
- the branched Attachment Group Linker (X B ) is directly attached to Tethering Group (T).
- T Tethering Group
- Typical branched Attachment Group Linkers are, for example, amino acids that include an additional functional group in their side chain that provide an easy means for covalently attaching the branched Attachment Group Linker and the Tethering Group. Suitable amino acids include, but are not limited to, lysine, aspartic acid, glutamic acid, serine, threonine, asparagine, and glutamine.
- the branched Attachment Group Linker is lysine.
- the amino position on each amino acid is independently substituted with a methyl group.
- an amino acid unit is not required. So long as the Attachment Group Linker comprises chemical groups for covalent attachment to the two or more Attachment Groups (Q 1 and Q 2 ) in the Linker Assembly Unit, said group is a suitable component in a Linking Assembly Unit.
- the Linking Assembly Units are Optional Linking Groups (L 1 and L 2 ), which may be included for reasons such as facilitating attachment of the Drug Units to the LA Unit, or for introducing a cleavable linking group.
- the Drug Linking Assembly (DLA) Units of the present disclosure include an Optional Linking Group between the Drug Unit and the Attachment Group (Q 1 or Q 2 ).
- Q 1 or Q 2 the Attachment Group
- linkers are known in the art for attachment of Drug Units to functional groups present in antibodies or sites on linkers - and are useful herein for attaching Drug Units to the Attachment Groups of the Linking Assembly Unit.
- Optional Linking Groups include a terminal maleimide, allowing for reliable linkage between the attachment unit Q 1 or Q 2 . It is understood that the terminal maleimide functional groups are most useful for covalent attachment to Q 1 or Q 2 moieties that include a nucleophilic group such as hydroxyl, thiol, or amine and in particular an antibody thiol.
- an attached succinimide obtained from a maleimide-containing Tethering Group, exists in some embodiments, in hydrolyzed form(s), or when a basic group such as an amine is located proximal to a substituted succinimide, the succinimide is capable of reacting to form a self-stabilizing assembly (as described in further detail in WO 2013/173337).
- an Optional Linking Groups include a para-aminobenzyloxy- carbonyl (PABC) group that is covalently attached to a Drug Unit (D 1 or D 2 ).
- an Optional Linking Group has Formula (VIII) or (IX):
- R 1 * is hydrogen or a protecting group
- n is 1 or 2
- p is an integer from 1-5
- the phenylene in the previous mentioned groups may be optionally substituted with a sugar such as glucose, or a derivative thereof.
- the amine groups of R 24 optionally include a methyl (CH 3 ) instead of an H.
- R 24 is a di-, or tri-peptide.
- the amino acids of the peptide unit in R 24 are independently selected from valine, alanine, glycine, leucine, and citrulline. It is understood that the Formulae above are shown before linkage to Attachment Groups (X). The "wavy line" indicates the point of attachment to the Drug Unit.
- an Optional Linking Group has Formula (XI) or (XII):
- R 1 * is hydrogen or a protecting group
- subscript n is 1 or 2
- subscript p is an integer from 1-5
- -(di-peptide)-NH-phenylene-CH 2 -0-C( 0)-heterocylyl-C 1- ⁇ lkylene-b ⁇ heterocyclyl-b 2 -
- b 1 and b 2 are independently a bond or heteroatoms selected from NH or O
- the each heterocyclyl group is a 5 or 6 membered ring having 1- 3 heteroatom ring members selected from N, O, and S
- each heterocyclyl group is optionally substituted with from 1 to 3 groups selected from C 1-4 alkyl, hydroxyl, alkoxy
- b 1 and b 2 are each heteroatoms selected from NH or O.
- the amine groups of R 24 may also include a methyl (CH 3 ) instead of an H.
- R 24 is a di-, or tri-peptide.
- the amino acids of the peptide unit in R 24 are independently selected from valine, alanine, glycine, leucine, and citrulline. It is understood that the Formulae above are shown before covalent attachment to Attachment Groups (X). The "wavy line" indicates the point of attachment to Drug Unit D 1 or D 2 .
- Optional Linking Groups are Releaseable Linking Group, L R1 or L 112 .
- the Optional Linking Group does not include a Releaseable Linking Group.
- release of Drug Unit is via a total protein degradation pathway (i.e., non-cleavable pathway).
- the Optional Linking Group is a Releasable Linking Group (L R1 or L 112 ) that group allows efficient release of free drug at the target cell, sufficient to induce, e.g., cytotoxicity or cytostaticity.
- the Releasable Linking Group is designed for efficient release of the free drug once the conjugate has been internalized into the target cell, but may also be designed to release free drug within the vicinity of targeted cells. Suitable recognition sites for cleavage are those that allow efficient release of an MD- ADC's Drug Unit(s).
- the recognition site is a peptide cleavage site (such as in a peptide-based releasable linker assembly), a sugar cleavage site (such as in sugar-based releasable linker assembly, which is or is comprised of a Glucuronide Unit), or a disulfide cleavage site (such as in disulfide-based releasable linker assembly).
- peptide cleavage sites include those recognized by intracellular proteases, such as those present is lysosomes.
- sugar cleavage site include those recognized by glycosidases, including glucuronidases, such as beta- glucuronidase.
- the Releaseable Linking Group (L or L ) is a di-peptide.
- the di-peptide is -Val-Cit-, -Phe-Lys- or -Val-Ala-.
- L 1 and L 2 are independently selected from the group consisting of maleimido-caproyl (mc), maleimido-caproyl-valine-citrulline (mc-vc), maleimido-caproyl- valine-citrulline-paraaminobenzyloxycarbonyl (mc-vc-PABC) and MDPr-vc. It is understood that L 1 and L 2 in some embodiments is further substituted with a basic moiety such as an amine to form a self-stabilizing succinimide linker discussed above and in greater detail in (WO 2013/173337).
- auristatin and maytansine ADCs are currently in clinical development for the treatment of cancer.
- Monomethyl auristatin E is conjugated through a protease cleavable peptide linker to an antibody
- monomethyl auristatin F is conjugated directly to an antibody through maleimidocaproic acid
- DM1 is conjugated through a disulfide or directly through the heterobifunctional SMCC linker
- DM4 is conjugated through a disulfide linker.
- linker systems can be used with the MD-ADCs described herein and provide release of drug by an enzymatically cleavable or non-enzymatically cleavable system depending on the linker system used.
- Disulfide, thioether, peptide, hydrazine, ester, or carbamate bonds are all examples of bonds that are also useful for connecting Drug Unit D 1 or D 2 to a first or second Optional Linking Group (L 1 or L 2 ).
- Optional partitioning agents (Y) can be linked via any suitable atom of the Optional Linking Groups. Methods of making such linkages are known in the art.
- the MD-ADCs described herein can also include attached Partitioning Agents (Y).
- the Partitioning Agents are useful, for example, to mask the hydrophobicity of particular Drug Units or Linking Assembly Units. Accordingly, a number of Partitioning Agents will act to increase the hydrophilic character of the MD-ADC to which they are attached.
- Representative Partitioning Agents include polyethylene glycol (PEG) units, cyclodextrin units, polyamides, hydrophilic peptides, polysaccharides and dendrimers.
- PEG polyethylene glycol
- the optional Partitioning Agent is included in one or more of groups T, L 1 , L 2 , X, X 1 or X 2 , Q 1 or Q 2
- the Partitioning Agent in some embodiments includes a lysine residue which allows for covalent attachment of the Partitioning Agent to the Linking Assembly Unit.
- Polydisperse PEGS, monodisperse PEGS and discrete PEGs can be used to make the Compounds of the present invention.
- Polydisperse PEGs are a heterogeneous mixture of sizes and molecular weights whereas monodisperse PEGs are typically purified from heterogeneous mixtures and are therefore provide a single chain length and molecular weight.
- Preferred PEG Units are discrete PEGs, compounds that are synthesized in step-wise fashion and not via a polymerization process. Discrete PEGs provide a single molecule with defined and specified chain length.
- the PEG Unit provided herein comprises one or multiple polyethylene glycol chains.
- the polyethylene glycol chains can be linked together, for example, in a linear, branched or star shaped configuration.
- at least one of the PEG chains is derivitized at one end for covalent attachment to an appropriate site on a component of the Linking Assembly Unit (e.g. Q 1 , Q 2 , X, X 1 or X 2 , or to optional Linking Groups (L 1 or L 2 )).
- Exemplary attachments to the Linking Assembly Unit are by means of non-conditionally cleavable linkages or via
- attachments are via amide linkage, ether linkages, ester linkages, hydrazone linkages, oxime linkages, disulfide linkages, peptide linkages or triazole linkages.
- attachment to the Linking Assembly Unit is by means of a non-conditionally cleavable linkage.
- attachment to the Linking Assembly Unit is not via an ester linkage, hydrazone linkage, oxime linkage, or disulfide linkage.
- attachment to the Linking Assembly Unit is not via a hydrazone linkage.
- a conditionally cleavable linkage refers to a linkage that is not substantially sensitive to cleavage while circulating in the plasma but is sensitive to cleavage in an intracellular or intratumoral environment.
- a non-conditionally cleavable linkage is one that is not substantially sensitive to cleavage in any biological environment. Chemical hydrolysis of a hydrazone, reduction of a disulfide, and enzymatic cleavage of a peptide bond or glycosidic linkage are examples of conditionally cleavable linkages.
- the PEG Unit will be directly attached to the MD-ADC (or Intermediate thereof) at the Linking Assembly Unit.
- the other terminus (or termini) of the PEG Unit will be free and untethered and may take the form of a methoxy, carboxylic acid, alcohol or other suitable functional group.
- the methoxy, carboxylic acid, alcohol or other suitable functional group acts as a cap for the terminal PEG subunit of the PEG Unit.
- untethered it is meant that the PEG Unit will not be attached at that untethered site to a Drug Unit, to an antibody, or to a linking component linking a Drug Unit and/or an antibody.
- the multiple PEG chains may be the same or different chemical moieties (e.g., PEGs of different molecular weight or number of subunits).
- the multiple PEG chains are attached to the Linking Assembly Unit at a single attachment site.
- the PEG Unit in addition to comprising repeating
- polyethylene glycol subunits may also contain non-PEG material (e.g., to facilitate coupling of multiple PEG chains to each other or to facilitate coupling to the Linking Assembly Unit).
- Non- PEG material refers to the atoms in the PEG Unit that are not part of the repeating -CH 2 CH 2 0- subunits.
- the PEG Unit comprises two monomelic PEG chains attached to each other via non-PEG elements.
- the PEG Unit comprises two linear PEG chains attached to a central core that is attached to the Linking Assembly Unit (i.e., the PEG Unit itself is branched).
- Bioechnol 11:141- 142 PEGylation of an N-terminal a-carbon of a peptide with PEG-nitrophenylcarbonate ("PEG- NPC") or PEG-trichlorophenylcarbonate); and Veronese (2001) Biomaterials 22:405-417 (Review article on peptide and protein PEGylation)].
- PEG may be covalently bound to amino acid residues via a reactive group.
- Reactive groups are those to which an activated PEG molecule may be bound (e.g., a free amino or carboxyl group).
- N-terminal amino acid residues and lysine (K) residues have a free amino group
- C-terminal amino acid residues have a free carboxyl group.
- Sulfhydryl groups are also useful as a reactive group for attaching PEG.
- enzyme-assisted methods for introducing activated groups (e.g., hydrazide, aldehyde, and aromatic-amino groups) specifically at the C-terminus of a polypeptide have been described (see Schwarz, et al. (1990) Methods Enzymol. 184:160; Rose, et al. (1991) Bioconjugate Chem. 2:154; and Gaertner, et al. (1994) J. Biol Chem. 269:7224].
- PEG molecules are attached to amino groups using
- mPEG methoxylated PEG having different reactive moieties.
- reactive moieties include succinimidyl succinate (SS), succinimidyl carbonate (SC), mPEG- imidate, para-nitrophenylcarbonate (NPC), succinimidyl propionate (SPA), and cyanuric chloride.
- Non-limiting examples of such mPEGs include mPEG-succinimidyl succinate (mPEG- SS), mPEG 2 -succinimidyl succinate (mPEG 2 -SS); mPEG-succinimidyl carbonate (mPEG-SC), mPEG 2 -succinimidyl carbonate (mPEG 2 -SC); mPEG-imidate, mPEG-para-nitrophenylcarbonate (mPEG-NPC), mPEG-imidate; mPEG 2 -para-nitrophenylcarbonate (mPEG 2 -NPC); mPEG- succinimidyl propionate (mPEG-SPA); mPEG 2 -succinimidyl propionate (mPEG,—SPA);
- mPEG-N-hydroxy-succinimide mPEG-NHS
- mPEG 2 -N-hydroxy-succinimide mPEG 2 — NHS
- mPEG-cyanuric chloride mPEG 2 -cyanuric chloride
- mPEG 2 -Lysinol-NPC mPEG 2 -Lys- NHS
- the PEG Unit is functionalized so that it is capable of covalent attachment to the Linking Assembly Unit.
- Functionalization includes, for example, via an amine, thiol, NHS ester, maleimide, alkyne, azide, carbonyl, or other functional group.
- the PEG Unit further comprises non-PEG material (i.e., material not comprised of -CH 2 CH 2 0-) that provides coupling to its Linking Assembly Unit or coupling of two or more PEG chains.
- PEG polyethylene glycol
- the reactive PEG reagent will result in formation of a carbamate or amide bond upon attachment to the Linking Assembly Unit (e.g. Q 1 , Q 2 , X, X 1 or X 2 , or to optional Linking Groups (L 1 or L 2 )).
- the following PEG reagents are useful in various embodiments: mPEG 2 -NHS, mPEG 2 -ALD, multi-Arm PEG,
- mPEG(MAL) 2 mPEG 2 (MAL), mPEG-NH 2 , mPEG-SPA, mPEG-SBA, mPEG-thioesters, mPEG-Double Esters, mPEG-BTC, mPEG-ButyrALD, mPEG-ACET, heterofunctional PEGs (NH 2 -PEG-COOH, Boc-PEG-NHS, Fmoc-PEG-NHS, NHS-PEG-VS, NHS-PEG-MAL), PEG acrylates (ACRL-PEG-NHS), PEG-phospholipids (e.g., mPEG-DSPE), multiarmed PEGs of the SUNBRITETM series including the GL series of glycerine-based PEGs activated by a chemistry chosen by those skilled in the art, any of the SUNBRITE activated PEGs (including but not limited to carboxyl-PEGs, p-NP-PEGs (
- the presence of the PEG Unit in a Drug Linking Assembly Unit is capable of having two potential impacts upon the pharmacokinetics of the resulting MD-ADC.
- the desired impact is a decrease in clearance (and consequent increase in exposure) that arises from the reduction in non-specific interactions induced by the exposed hydrophobic elements of the Drug Unit.
- the second impact is undesired and is a decrease in volume and rate of distribution that sometimes arises from the increase in the molecular weight of the MD-ADC.
- Increasing the number of PEG subunits increases the hydrodynamic radius of a conjugate, typically resulting in decreased diffusivity.
- the PEG Unit comprises at least 6 subunits, at least 7 subunits, at least 8 subunits, at least 9 subunits, at least 10 subunits, at least 11 subunits, at least 12 subunits, at least 13 subunits, at least 14 subunits, at least 15 subunits, at least 16 subunits, at least 17 subunits, at least 18 subunits, at least 19 subunits, at least 20 subunits, at least 21 subunits, at least 22 subunits, at least 23 subunits, or at least 24 subunits.
- a subunit of a PEG Unit refers to a polyethylene glycol moiety having the formula
- the PEG Unit comprises no more than about
- the PEG Unit comprises one or more linear PEG chains each having at least 2 subunits, at least 3 subunits, at least 4 subunits, at least 5 subunits, at least 6 subunits, at least 7 subunits, at least 8 subunits, at least 9 subunits, at least 10 subunits, at least 11 subunits, at least 12 subunits, at least 13 subunits, at least 14 subunits, at least 15 subunits, at least 16 subunits, at least 17 subunits, at least 18 subunits, at least 19 subunits, at least 20 subunits, at least 21 subunits, at least 22 subunits, at least 23 subunits, or at least 24 subunits.
- the PEG Unit comprises a combined total of at least 6 subunits, at least 8, at least 10 subunits, or at least 12 subunits. In some such embodiments, the PEG Unit comprises no more than a combined total of about 72 subunits, preferably no more than a combined total of about 36 subunits.
- the PEG Unit comprises a combined total of from 4 to 72, 4 to 60, 4 to 48, 4 to 36 or 4 to 24 subunits, from 5 to 72, 5 to 60, 5 to 48, 5 to 36 or 5 to 24 subunits, from 6 to 72, 6 to 60, 6 to 48, 6 to 36 or from 6 to 24 subunits, from 7 to 72, 7 to 60, 7 to 48, 7 to 36 or 7 to 24 subunits, from 8 to 72, 8 to 60, 8 to 48, 8 to 36 or 8 to 24 subunits, from
- 9 to 72, 9 to 60, 9 to 48, 9 to 36 or 9 to 24 subunits from 10 to 72, 10 to 60, 10 to 48, 10 to 36 or 9 to 24 subunits, from 10 to 72, 10 to 60, 10 to 48, 10 to 36 or 9 to 24 subunits, from 10 to 72, 10 to 60, 10 to 48, 10 to 36 or 9 to 24 subunits, from 10 to 72, 10 to 60, 10 to 48, 10 to 36 or 9 to 24 subunits, from 10 to 72, 10 to 60, 10 to 48, 10 to 36 or 9 to 24 subunits, from 10 to 72, 10 to 60, 10 to 48, 10 to 36 or 9 to 24 subunits, from 10 to 72, 10 to 60, 10 to 48, 10 to 36 or 9 to 24 subunits, from 10 to 72, 10 to 60, 10 to 48, 10 to 36 or 9 to 24 subunits, from 10 to 72, 10 to 60, 10 to 48, 10 to 36 or 9 to 24 subunits, from 10 to 72, 10 to 60, 10 to 48, 10 to 36
- 10 to 24 subunits from 11 to 72, 11 to 60, 11 to 48, 11 to 36 or 11 to 24 subunits, from 12 to 72, 12 to 60, 12 to 48, 12 to 36 or 12 to 24 subunits, from 13 to 72, 13 to 60, 13 to 48, 13 to 36 or 13 to 24 subunits, from 14 to 72, 14 to 60, 14 to 48, 14 to 36 or 14 to 24 subunits, from 15 to 72, 15 to 60, 15 to 48, 15 to 36 or 15 to 24 subunits, from 16 to 72, 16 to 60, 16 to 48, 16 to 36 or 16 to 24 subunits, from 17 to 72, 17 to 60, 17 to 48, 17 to 36 or 17 to 24 subunits, from 18 to 72, 18 to 60, 18 to 48, 18 to 36 or 18 to 24 subunits, from 19 to 72, 19 to 60, 19 to 48, 19 to 36 or 19 to 24 subunits, from 20 to 72, 20 to 60, 20 to 48, 20 to 36 or 20 to 24 subunits, from 21 to 72, 21 to 60
- the PEG Unit comprises one or more linear PEG chains having a combined total of from 4 to 72, 4 to 60, 4 to 48, 4 to 36 or 4 to 24 subunits, from 5 to 72, 5 to 60, 5 to 48, 5 to 36 or 5 to 24 subunits, from 6 to 72, 6 to 60, 6 to 48, 6 to 36 or 6 to 24 subunits, from 7 to 72, 7 to 60, 7 to 48, 7 to 36 or 7 to 24 subunits, from 8 to 72, 8 to 60, 8 to 48, 8 to 36 or 8 to 24 subunits, from 9 to 72, 9 to 60, 9 to 48, 9 to 36 or 9 to 24 subunits, from 10 to 72, 10 to 60, 10 to 48, 10 to 36 or 10 to 24 subunits, from 11 to 72, 11 to 60, 11 to 48, 11 to 36 or 11 to 24 subunits, from 12 to 72, 12 to 60, 12 to 48, 12 to 36 or 12 to 24 subunits, from 13 to 72, 13 to 60, 13
- the PEG Unit is a derivitized linear single PEG chain having at least 2 subunits, at least 3 subunits, at least 4 subunits, at least 5 subunits, at least 6 subunits, at least 7 subunits, at least 8 subunits, at least 9 subunits, at least 10 subunits, at least
- the PEG Unit is a derivitized linear single PEG chain having from 6 to 72, 6 to 60, 6 to 48, 6 to 36 or 6 to 24 subunits, from 7 to 72, 7 to 60, 7 to 48, 7 to 36 or 7 to 24 subunits, from 8 to 72, 8 to 60, 8 to 48, 8 to 36 or 8 to 24 subunits, from 9 to 72, 9 to 60, 9 to 48, 9 to 36 or 9 to 24 subunits, from 10 to 72, 10 to 60, 10 to 48, 10 to 36 or 10 to 24 subunits, from 11 to 72, 11 to 60, 11 to 48, 11 to 36 or 11 to 24 subunits, from 12 to 72, 12 to 60,
- 12 to 48, 12 to 36 or 12 to 24 subunits from 13 to 72, 13 to 60, 13 to 48, 13 to 36 or 13 to 24 subunits, from 14 to 72, 14 to 60, 14 to 48, 14 to 36 or 14 to 24 subunits, from 15 to 72, 15 to 60, 15 to 48, 15 to 36 or 15 to 24 subunits, from 16 to 72, 16 to 60, 16 to 48, 16 to 36 or 16 to 24 subunits, from 17 to 72, 17 to 60, 17 to 48, 17 to 36 or 17 to 24 subunits, from 18 to 72, 18 to 60, 18 to 48, 18 to 36 or 18 to 24 subunits, from 19 to 72, 19 to 60, 19 to 48, 19 to 36 or 19 to 24 subunits, from 20 to 72, 20 to 60, 20 to 48, 20 to 36 or 20 to 24 subunits, from 21 to 72, 21 to 60, 21 to 48, 21 to 36 or 21 to 24 subunits, from 22 to 72, 22 to 60, 22 to 48, 22 to 36 or 22 to 24 subunits,
- the PEG Unit is a derivitized linear single PEG chain having from 2 to 72, 2 to 60, 2 to 48, 2 to 36 or 2 to 24 subunits, from 2 to 72, 2 to 60, 2 to 48, 2 to 36 or 2 to 24 subunits, from 3 to 72, 3 to 60, 3 to 48, 3 to 36 or 3 to 24 subunits, from 3 to 72, 3 to 60, 3 to 48, 3 to 36 or 3 to 24 subunits, from 4 to 72, 4 to 60, 4 to 48, 4 to 36 or 4 to 24 subunits, from 5 to 72, 5 to 60, 5 to 48, 5 to 36 or 5 to 24 subunits.
- Exemplary linear PEG Units that are useful as a Partitioning Agent in any of the embodiments provided herein are as follows:
- R 20 (CH 2 CH 2 0) n .
- R 22 -(CH 2 CH 2 0) n .
- R 21 wherein the wavy line indicates site of attachment to the Parallel Connector Unit
- R 20 is a PEG Attachment Unit
- R 21 i is a PEG Capping Unit; is an PEG Coupling Unit (i.e., for coupling multiple PEG subunit chains together)
- subscript n is independently selected from 2 to 72 ( preferably from 4 to 72, more preferably from 6 to 72, from 8 to 72, from 10 to 72, from 12 to 72 or from 6 to 24);
- subscript e is 2 to 5 each subscript n' is independently selected from 1 to 72.
- subscript n is 8 or about 8, 12 or about 12, 24 or about 24.
- the PEG Attachment Unit is part of the PEG Unit and that covalently attaches the PEG Unit to other portions of the Linking Assembly Units. Accordingly, a portion of the Linking Assembly Unit (T, Q 1 , L 1 , D 1 , X, Q 2 , L 2 , D 2 , X 1 or X 2 ) has a functional group that provides a bond to the PEG Unit.
- Functional groups for attachment of the PEG Unit to a site on the Linking Assembly Unit include sulfhydryl groups to form disulfide bonds or thioether bonds, aldehyde, ketone, or hydrazine groups to form hydrazone bonds, hydroxylamine to form oxime bonds, carboxylic or amino groups to form peptide bonds, carboxylic or hydroxy groups to form ester bonds, sulfonic acids to form sulfonamide bonds, alcohols to form carbamate bonds, and amines to form sulfonamide bonds or carbamate bonds or amide bonds.
- the PEG unit is covalently attached to a site on the Linking Assembly Unit, for example, via disulfide, thioether, hydrazone, oxime, peptide, ester, sulfonamide, carbamate, or amide bonds.
- the PEG Attachment Unit is attached by means of Click chemistry (a product of the cycloaddition between azide and alkyne functional groups), addition reaction, addition/elimination or substitution reaction that occurs when attaching the PEG Unit to the Linking Assembly Unit.
- the PEG Coupling Unit is part of the PEG Unit and is non-PEG material that acts to connect two or more chains of repeating CH 2 CH 2 0- subunits.
- the PEG coupling Unit R 22 is -C 1-10 alkylene-C(0)-NH-, -C 1-10 alkylene-NH-C(O)-, -C 2-10 alkylene- NH-, -C 2-1 oalkylene-0- , -Ci-io alkylene-S-, or -C 2-1 oalkylene-NH-.
- the PEG Attachment Unit R 20 is -C(O)-, -0-, -S-, -S(O)-, -NH-, -C(0)0-, -C(O)C 1-10 alkyl, -C(O)C 1-10 alkyl-O-, -C(O)C 1-10 alkyl-CO 2 -, -C(O)C 1-10 alkyl- NH-, -C(O)C 1-10 alkyl-S-, -C(O)C 1-10 alkyl-C(O)-NH-, -C(O)C 1-10 alkyl-NH-C(O)-, -C 1-10 alkyl, - C 1-10 alkyl-O-, -C 1-10 alkyl-CO 2 -, -C 1-10 alkyl-NH-, -C 1-10 alkyl-S-, -C 1-10 alkyl-C(O)-NH-, -C 1-10 alkyl-S-
- each R 21 is independently -C 1-10 alkyl, -C 2-10 alkyl-C0 2 H, -C 2-10 alkyl-OH, -C 2-10 alkyl-NH 2 , C 2-10 alkyl-NH(C 1-3 alkyl), or C 2-1 o alkyl-N(C 1-3 alkyl) 2; and each R 22 is independently -CMO alkyl- C(0)-NH-, -C 1-10 alkyl-NH-C(O)-, -C 2-10 alkyl-NH-, -C 2-10 alkyl-O- , -C 1-10 alkyl-S-, or -C 2-10 alkyl-NH-.
- R 20 -NH-, -C( 0)- , triazole-linked groups, or -S-, or
- R 21 is C 1-10 alkyl, -C 2-1 o alkyl-C0 2 H, -C 2-1 o alkyl-OH, or - C 2-10 alkyl-NH 2 .
- Illustrative linear PEG Units that can be used in any of the embodiments provided herein are as follows:
- the PEG Unit is added to the terminal attachment group (Q) of the Linking Assembly Unit. This can be achieved using a derivitized PEG unit with a terminal amine.
- the derivitized PEG with a terminal amine is linked to the terminal attachment group (Q) of the linking assembly unit via 1-3 amino acids (e.g. a mono-, di- , or tri-peptide).
- the PEG Unit is linked to the terminal attachment group (Q) with a formula of: Q-glycine-PEG unit.
- the PEG Unit is selected such that it improves clearance of the resultant MD-ADC but does not significantly impact the ability of the Conjugate to penetrate into the tumor.
- the Drug Unit and Linking Assembly Unit of the MD- ADC has a hydrophobicity comparable to that of a maleimido glucuronide MMAE drug-linker
- the PEG unit to be selected for use will preferably have from 8 subunits to about 24 subunits, more preferably about 12 subunits.
- the PEG Unit is from about 300 daltons to about 5 kilodaltons; from about 300 daltons, to about 4 kilodaltons; from about 300 daltons, to about 3 kilodaltons; from about 300 daltons, to about 2 kilodaltons; or from about 300 daltons, to about 1 kilodalton.
- the PEG Unit has at least 6 subunits or at least 8, 10 or 12 subunits.
- the PEG Unit has at least 6 subunits or at least 8, 10 or 12 subunits but no more than 72 subunits, preferably no more than 36 subunits.
- the number of subunits can represent an average number, e.g., when referring to a population of MD-ADCs or Intermediate Compounds, and using polydisperse PEGs.
- the LA Unit includes Optional Linking Groups (L 1 and L 2 ). It is understood that the Optional Linking Group may be attached to the drug moiety prior to LA Unit attachment, or the Optional Linking Group may be attached to the LA Unit prior to drug moiety attachment.
- the Drug Unit (D) is that of a cytotoxic or cytostatic drug, also referred to herein as a cytotoxic or cytostatic agent.
- the Drug Unit has an atom that provides a covalent bond with the first or second Attachment Group (Q 1 or Q 2 ).
- the Drug Unit (D 1 or D 2 ) has a nitrogen atom that can form a bond with the first or second Attachment Group (Q 1 or Q 2 ), respectivly.
- the Drug Unit (D 1 or D 2 ) has a carboxylic acid moiety providing a bond with the first or second Attachment Group (Q 1 or Q 2 ).
- the Drug Unit (D 1 or D 2 ) contains a sulfhydryl functional group residue that provides a bond with the first or second Attachment Group (Q 1 or Q 2 ).
- the Drug Unit has a hydroxyl or ketone functional group residue that provides a bond with the first or second Attachment Group (Q 1 or Q 2 ).
- Useful classes of cytotoxic agents include, for example, antitubulin agents, DNA minor groove binders, DNA replication inhibitors, alkylating agents, antibiotics, antifolates, antimetabolites, chemotherapy sensitizers, topoisomerase inhibitors, vinca alkaloids, or the like.
- Particularly examples of useful classes of cytotoxic agents include, for example, DNA minor groove binders, DNA alkylating agents, and tubulin inhibitors.
- Exemplary cytotoxic agents include, for example, auristatins, camptothecins, duocarmycins, etoposides, maytansines and maytansinoids, taxanes, benzodiazepines or benzodiazepine containing drugs (e.g., pyrrolo[l,4]- benzodiazepines (PBDs), indolinobenzodiazepines, and oxazolidinobenzodiazepines) and vinca alkaloids.
- PBDs pyrrolo[l,4]- benzodiazepines
- indolinobenzodiazepines e.g., indolinobenzodiazepines
- oxazolidinobenzodiazepines e.g., vinca alkaloids.
- Select benzodiazepine containing drugs are described in WO 2010/091150, WO 2012/112708, WO 2007/085930, and WO 2011/023883.
- At least one Drug Unit is an auristatin. In some embodiments, all Drugs Units are auristatins. In some embodiments, at least one Drug Unit is MMAE, Auristatin T, MMAF or Dolastatin 10. In some embodiments, all Drug Units are MMAE, Auristatin T, MMAF or Dolastatin 10. In some embodiments, the Drug Units are MMAE and MMAF.
- At least one Drug Unit is MMAE, camptothecin, Superdox, Dolastatin 10, Vinblastine and Ciprofloxacin.
- the cytotoxic agent is maytansine or a maytansinoid (e.g., DM1, DM4) another group of anti-tubulin agents.
- a maytansinoid e.g., DM1, DM4
- the Drug is a benzodiazepine (including benzodiazepine containing drugs e.g., pyrrolo[l,4]benzodiazepines (PBDs), indolinobenzodiazepines, and oxazolidinobenzodiazepines).
- PBDs pyrrolo[l,4]benzodiazepines
- indolinobenzodiazepines e.g., indolinobenzodiazepines
- oxazolidinobenzodiazepines e.g., oxazolidinobenzodiazepines
- PBDs are of the general structure:
- PBDs to form an adduct in the minor groove enables them to interfere with DNA processing, hence their use as antitumor agents.
- the biological activity of these molecules are sometimes potentiated by, for example, joining two PBD units together through their C8/C'-hydroxyl functionalities via a flexible alkylene linker.
- the PBD dimers are thought to form sequence-selective DNA lesions such as the palindromic 5'-Pu-GATC-Py-3' interstrand cross-link which is thought to be mainly responsible for their biological activity.
- the Drug Unit (D 1 or D 2 ), in some embodiments, are of different auristatin or non- auristatin conjugated drugs having a hydrophobicity comparable to or greater than monomethyl auristatin E.
- the two different Drug Units are selected so that the IC50 values of the D 1 and D 2 are within 1 to 2 log units, more preferably with 0.5 to 1 log units, of each other, or have a disparity between these values that are compensatable by appropriate selection of the D 1 ⁇ 2 ratio on a DLA so that an effective amount of each drug is being simultaneously or near simultaneously delivered to the desired sites of intracellular action.
- D 1 or D 2 is of MMAE or an auristatin having a hydrophobicity comparable to or greater than monomethyl auristatin E.
- the D 1 or D 2 auristatin Drug Unit is covalently attached to a first or second Attachment Group (Q 1 or Q 2 ), respectively, for example, via its N or C terminus.
- MMAE has a SlogP value of 2.59.
- drugs to be used as D 1 or D 2 Drug Units in the present invention will have a SlogP value of 1.5 or greater, 2.0 or greater, or 2.5 or greater.
- drugs to be used as D 1 or D 2 Drug Units in the present invention will have a SlogP value from (a) about 1.5, about 2, or 2.5 to about 7, (b) about 1.5, about 2, or 2.5 to about 6, (c) about 1.5, about 2 or about 2.5 to about 5, (d) about 1.5, about 2, or 2.5 to about 4, or (e) about 1.5, about 2 or about 2.5 to about 3.
- An auristatin D 1 or D 2 Drug Unit preferably has Formula DE as shown below wherein attachment to the first or second Attachment Group (Q 1 or Q 2 ) is via the N terminus:
- R 2 is selected from the group consisting of H and d-C 8 alkyl
- R 3 is selected from the group consisting of H, d-C 8 alkyl, C 3 -C 8 carbocycle, aryl,
- R 4 is selected from the group consisting of H, d-C 8 alkyl, C 3 -C 8 carbocycle, aryl, d-C 8 alkyl-aryl, d-C 8 alkyl-(C 3 -C 8 carbocycle), C 3 -C 8 heterocycle and d-C 8 alkyl-(C 3 -C 8 heterocycle);
- R 5 is selected from the group consisting of H and methyl
- R 4 and R 5 jointly form a carbocyclic ring and have the
- R a and R are independently selected from the group consisting of H, d-C 8 alkyl and C 3 -C 8 carbocycle and n is selected from the group consisting of 2, 3, 4, 5 and 6;
- R 6 is selected from the group consisting of H and d-C 8 alkyl
- R 7 is selected from the group consisting of H, d-C 8 alkyl, C 3 -C 8 carbocycle, aryl, d-C 8 alkyl-aryl, d-C 8 alkyl-(C 3 -C 8 carbocycle), C 3 -C 8 heterocycle and d-C 8 alkyl-(C 3 -C 8 heterocycle);
- each R 8 is independently selected from the group consisting of H, OH, d-C 8 alkyl, C 3 -C 8 carbocycle and 0-(d-C 8 alkyl);
- R 9 is selected from the group consisting of H and d-C 8 alkyl
- R 18 is selected from the group consisting of-C(R 8 ) 2 -C(R 8 ) 2 -aryl, -C(R 8 ) 2 -C(R 8 ) 2 -(C 3 -C 8 heterocycle), and -C(R 8 ) 2 -C(R 8 ) 2 -(C 3 -C 8 carbocycle).
- MMAE conjugated via its N terminus is shown below:
- the D 1 or D 2 Drug Unit is that of a vinca compound, a camptothecin or a anthracyclin cytotoxic compound.
- D 1 and D 2 are a drug pair selected from the group consisting of MMAE/MMAF, MMAE/camptothecin, Superdox/camptothecin, Superdox/MMAE, Dolastatin 10/MMAE, Dolastatin 10/MMAF, Vinblastine/MMAE, and Vinblastine/MMAF.
- incorporation assay is used. For example, cells at a density of 5,000 cells/well of a 96-well plated is cultured for a 72-hour period and exposed to 0.5 ⁇ of 3 H-thymidine during the final 8 hours of the 72-hour period, and the incorporation of 3 H-thymidine into cells of the culture is measured in the presence and absence of MD-ADC.
- the MD-ADC has a cytostatic or cytotoxic effect on the cell line if the cells of the culture have reduced 3 H-thymidine incorporation compared to cells of the same cell line cultured under the same conditions but not contacted with the MD-ADC.
- cell viability is measured by determining in a cell the uptake of a dye such as neutral red, trypan blue, or ALAMARTM blue (see, e.g., Page et al., 1993, Intl. J. of Oncology 3:473-476).
- a dye such as neutral red, trypan blue, or ALAMARTM blue
- the cells are incubated in media containing the dye, the cells are washed, and the remaining dye, reflecting cellular uptake of the dye, is measured spectrophotometrically.
- the protein-binding dye sulforhodamine B can also be used to measure cytoxicity (Skehan et al, 1990, J. Nat'l Cancer Inst. 82: 1107-12).
- Preferred MD-ADCs include those with an IC50 value (defined as the niAB concentration that gives 50% cell kill) of less than 1000 ng/ml, preferably less than 500 ng/ml, more preferably less than 100 ng/ml, even most preferably less than 50 or even less than 10 ng/ml on the cell line.
- Antibodies useful in the MD-ADCs described herein are essentially any antibodies having four available inter-chain disulfide linkages, or the eight thiols that are produced by reduction of those inter-chain disulfide linkages for MD-ADCs having D 1 + D 2 ranging from 2 to 16 when in 1 : 1 ratio.
- the antibodies are generally non-engineered antibodies - antibodies in which no modifications are made to introduce additional amino acids or peptides, but in some embodiments are genetically engineered to contain a conjugatable cysteine residue for MD- ADCs having D 1 + D 2 ranging from 2 to 32 when in 1 : 1 ratio.
- the antibodies of the present disclosure include one or more engineered cysteine (eCys) residues.
- eCys residue is a cysteine amino acid or a derivative thereof that is incorporated into the heavy chain or light chain of an antibody, typically the one or more eCys residues are incorporated into the antibody by mutagenizing the parent antibody. Further information can be found in U.S. Pat. No. 9,000,130, the contents of which is incorporated herein for all purposes.
- derivatives of cysteine (Cys) include, but are not limited to beta-2-Cys, beta-3-Cys, homocysteine, and N-methyl cysteine.
- MD-ADCs multi-drug antibody drug conjugates
- Ab is an antibody that is a non-engineered antibody
- T is a Tethering Group attached to a the sulfur atom of a thiol produced by reduction of the antibody's interchain disulfide linkages;
- Q 1 is a first Attachment Group
- Q 2 is a second Attachment Group
- X is an Attachment Group Linker
- D 1 is a first Drug Unit
- D 2 is a second Drug Unit
- L 1 is an Optional Linking Group joining D 1 to Q 1 ;
- L 2 is an Optional Linking Group joining D 2 to Q 2 ;
- subscripts m 1 and m 2 are each independently 0 or 1;
- Y is a Partitioning Agent
- n 0 or 1.
- the MD-ADC is represented by formula (II):
- Ab is an antibody that is a non-engineered antibody
- T is a Tethering Group attached to the sulfur atom of a thiol produced by reduction of the antibody's interchain disulfide linkages
- Q 1 is a first Attachment Group
- Q 2 is a second Attachment Group
- X is an Attachment Group Linker
- D 1 is a first Drug Unit
- D 2 is a second Drug Unit
- L 1 is an Optional Linking Group joining D 1 to Q 1 ;
- L 2 is an Optional Linking Group joining D 2 to Q 2 ;
- subscripts m 1 and m 2 are each independently 0 or 1;
- Y is a Partitioning Agent; and subscript n is 0 or 1.
- the MD-ADC is represented by the Formula (III):
- Ab is an antibody that is a non-engineered antibody
- T is a Tethering Group attached to a sulfur atom of a thiol produced by reduction of the
- each Q 1 is an independently selected first Attachment Group
- Q 2 is a second Attachment Group
- X 1 and X 2 are each an independently selected Attachment Group Linker
- D 1 is a first Drug Unit
- D 2 is a second Drug Unit
- each L 1 is an independently selected Optional Linking Group joining D 1 to Q 1 ;
- L 2 is an Optional Linking Group joining D 2 to Q 2 ;
- m 1 and m 2 are each independently 0 or 1;
- Y is a Partitioning Agent
- n 0 or 1.
- the MD-ADC is represented by the Formula (IV):
- Ab is an antibody that is a non-engineered antibody
- T is a Tethering Group attached to a sulfur atom of a thiol produced by reduction of the
- Q 1 is an first Attachment Group
- each Q 2 is an independently selected second Attachment Group
- X 1 and X 2 are each an independently selected Attachment Group Linker
- D 1 is a first Drug Unit
- D 2 is a second Drug Unit
- L 1 is an Optional Linking Group joining D 1 to Q 1 ;
- each L 2 is an independently selected Optional Linking Group joining D 2 to Q 2 ;
- subscripts m 1 and m 2 are each independently 0 or 1;
- Y is a Partitioning Agent that is attached to a site on L, Q 1 , X 1 , X 2 , Q 2 , L 1 or L 2 ;
- n 0 or 1.
- L, Q 1 , Q 2 , X 1 , X 2 , L 1 , L 2 , D 1 , D 2 , and Y are as described in the preceding sections.
- suitable antibodies are those that are intact or fully-reduced antibodies.
- the term 'fully-reduced' is meant to refer to antibodies in which all four inter-chain disulfide linkages have been reduced to provide eight thiols that can be attached to Tethering Groups (T).
- Ab* is an antibody that comprises one or more engineered cysteine (eCys) residues, the eCys residues are free so that the thiols can be attached to the Tethering Group(s) (T).
- T is a Tethering Group attached to a sulfur atom of an engineered cysteine or derivative thereof in an antibody's heavy chain or light chain, and in some embodiments is also attached to thiol(s) produced by reduction of interchain disulfide linkages in said antibody.
- the antibody is directed against a cancer cell antigen. In another group of embodiments, the antibody is directed against a bacteria-related antigen. In yet another group of embodiments, the antibody is directed against an autoimmune cell antigen.
- Useful polyclonal antibodies are heterogeneous populations of antibody molecules derived from the sera of immunized animals.
- Useful monoclonal antibodies are homogeneous populations of antibodies to a particular antigenic determinant (e.g., a cancer cell antigen, a viral antigen, a microbial antigen, a protein, a peptide, a carbohydrate, a chemical, nucleic acid, or fragments thereof).
- a monoclonal antibody (mAb) to an antigen-of-interest can be prepared by using any technique known in the art which provides for the production of antibody molecules by continuous cell lines in culture.
- Useful monoclonal antibodies include, but are not limited to, human monoclonal antibodies, humanized monoclonal antibodies, or chimeric human-mouse (or other species) monoclonal antibodies.
- the antibodies include full-length antibodies and antigen binding fragments thereof.
- Human monoclonal antibodies may be made by any of numerous techniques known in the art (e.g., Teng et al, 1983, Proc. Natl. Acad. Sci. USA. 80:7308-7312; Kozbor et al, 1983, Immunology Today 4:72-79; and Olsson et al, 1982, Meth. Enzymol. 92:3-16).
- the antibody can be a functionally active fragment, derivative or analog of an antibody that immunospecifically binds to target cells (e.g., cancer cell antigens, viral antigens, or microbial antigens) or other antibodies bound to tumor cells or matrix.
- target cells e.g., cancer cell antigens, viral antigens, or microbial antigens
- other antibodies bound to tumor cells or matrix.
- “functionally active” means that the fragment, derivative or analog is able to immunospecifically binds to target cells.
- synthetic peptides containing the CDR sequences can be used in binding assays with the antigen by any binding assay method known in the art (e.g., the BIA core assay) (See, e.g., Kabat et al, 1991, Sequences of Proteins of Immunological Interest, Fifth Edition, National Institute of Health, Bethesda, Md; Kabat E et al, 1980, J. Immunology 125(3):961-969).
- recombinant antibodies such as chimeric and humanized monoclonal antibodies, comprising both human and non-human portions, which are preferably made using standard recombinant DNA techniques, are useful antibodies.
- a chimeric antibody is a molecule in which different portions are derived from different animal species, such as for example, those having a variable region derived from a murine monoclonal and human immunoglobulin constant regions. (See, e.g., U.S. Patent No. 4,816,567; and U.S. Patent No.
- Humanized antibodies are antibody molecules from non-human species having one or more complementarity determining regions (CDRs) from the non-human species and a framework region from a human immunoglobulin molecule.
- CDRs complementarity determining regions
- Such chimeric and humanized monoclonal antibodies are preferably produced by recombinant DNA techniques known in the art, for example using methods described in International Publication No. WO 87/02671; European Patent Publication No. 0 184 187;
- Completely human antibodies are particularly desirable and are preferably produced using transgenic mice that are incapable of expressing endogenous immunoglobulin heavy and light chains genes, which in some embodiments express human heavy and light chain genes.
- Antibodies immunospecific for a cancer cell antigen are preferably obtained commercially or produced by any method known to one of skill in the art such as, e.g., chemical synthesis or recombinant expression techniques.
- the nucleotide sequence encoding antibodies immunospecific for a cancer cell antigen is sometimes obtained, e.g., from the GenBank database or a database like it, the literature publications, and othertimes obtained by routine cloning and sequencing.
- Antibodies immunospecific for a cancer cell antigen are sometimes obtained commercially and othertimes produced by any method known to one of skill in the art such as, e.g., recombinant expression techniques.
- the nucleotide sequence encoding antibodies immunospecific for a cancer cell antigen is sometimes obtained, e.g., from the GenBank database or a database like it, the literature publications, and othertimes by routine cloning and sequencing.
- useful antibodies can bind to a receptor or a receptor complex expressed on an activated lymphocyte.
- the receptor or receptor complex can comprise an immunoglobulin gene superfamily member, a TNF receptor superfamily member, an integrin, a cytokine receptor, a chemokine receptor, a major histocompatibility protein, a lectin, or a complement control protein.
- the antibody will specifically bind CD19, CD20, CD30, CD33, CD70, alpha- v-beta-6, Liv-1 or Lewis Y antigen.
- the anti-CD30 antibody can be, for example, the chimeric AC10 antibody, brentuximab.
- the anti-CD30 antibody can have a heavy chain variable region having the amino acid sequence set forth in SEQ ID NO:l, a light chain variable region having the amino acid sequence set forth in SEQ ID NO:2, a human gamma I constant region having the amino acid sequence set forth in SEQ ID NO:7 and a human kappa constant region having the amino acid sequence set forth in SEQ ID NO:8.
- the anti-CD30 antibody preferably is a humanized AC 10 antibody or has a heavy chain variable region having the amino acid sequence set forth in SEQ ID NO:9, a light chain variable region having the amino acid sequence set forth in SEQ ID NO: 10.
- that antibody further comprises a human gamma I constant region having the amino acid sequence set forth in SEQ ID NO:7 optionally having a serine to cysteine substitution at position 239 (according to the EU index) and a human kappa constant region having the amino acid sequence set forth in SEQ ID NO: 8.
- the anti-CD70 antibody is preferably a humanized antibody (see, e.g., US 20140060600A1 ).
- the anti-CD70 antibody has a heavy chain variable region having the amino acid sequence set forth in SEQ ID NO:3, and a light chain variable region having the amino acid sequence set forth in SEQ ID NO:4.
- the anti-CD19 antibody is preferably a humanized antibody (see, e.g., US 20140060600A1 ).
- the hBU12 antibody has a heavy chain variable region having the amino acid sequence set forth in SEQ ID NO:5, and a light chain variable region having the amino acid sequence set forth in SEQ ID NO: 6.
- Another preferred antibody is a humanized anti-CD33 antibody (US 2013/0309223 incorporated by reference herein in its entirety and for all purposes), a humanized anti-Beta6 antibody (see, e.g., WO 2013/123152 incorporated by reference herein in its entirety and for all purposes), a humanized anti-Liv-1 antibody (see, e.g., US 2013/0259860 incorporated by reference herein in its entirety and for all purposes), or a humanized AC 10 antibody (see, e.g., US 8,257,706 incorporated by reference herein in its entirety and for all purposes).
- Exemplary attachments to the antibody is via thioether linkages.
- antibodies available for the treatment of cancer include, but are not limited to, humanized anti-HER2 monoclonal antibody, HERCEPTIN® (trastuzumab; Genentech) for the treatment of patients with metastatic breast cancer; RITUXAN® (rituximab; Genentech) which is a chimeric anti-CD20 monoclonal antibody for the treatment of patients with non-Hodgkin's lymphoma; OvaRex (AltaRex Corporation, MA) which is a murine antibody for the treatment of ovarian cancer; Panorex (Glaxo Wellcome, NC) which is a murine IgG 2a antibody for the treatment of colorectal cancer; Cetuximab Erbitux (Imclone Systems Inc., NY) which is an anti- EGFR IgG chimeric antibody for the treatment of epidermal growth factor positive cancers, such as head and neck cancer; Vitaxin (Medlmmune, Inc., MD) which is a humanized anti-HER2
- antibodies useful in the treatment of cancer include, but are not limited to, antibodies against the following antigens: CA125 (ovarian), CA15-3 (carcinomas), CA19-9 (carcinomas), L6 (carcinomas), Lewis Y (carcinomas), Lewis X (carcinomas), alpha fetoprotein (carcinomas), CA 242 (colorectal), placental alkaline phosphatase (carcinomas), prostate specific antigen (prostate), prostatic acid phosphatase (prostate), epidermal growth factor (carcinomas), MAGE-1 (carcinomas), MAGE-2 (carcinomas), MAGE-3 (carcinomas), MAGE -4
- carcinoma tumor cells
- anti-transferrin receptor carcinomas
- p97 melanoma
- MUC1-KLH breast cancer
- CEA colonrectal
- gplOO melanoma
- MARTI melanoma
- PSA prostate
- IL-2 receptor T-cell leukemia and lymphomas
- CD20 non-Hodgkin's lymphoma
- CD52 non-Hodgkin's lymphoma
- Some specific, useful antibodies include, but are not limited to, BR96 mAb (Trail, P. A., Willner, D., Lasch, S. J., Henderson, A. J., Hofstead, S. J., Casazza, A. M., Firestone, R. A., Hellstrom, I., Hellstrom, K.
- mAbs against the CD70 antigen such as 1F6 mAb and 2F2 mAb
- mAbs against the CD30 antigen such as AC10
- Many other internalizing antibodies that bind to tumor associated antigens can be used and have been reviewed (Franke, A.
- the Drug Linking Assembly Unit represented by Formulas lb, lib, lib, or IVb, wherein T comprises a maleimido group, and each of X, X 1 , X 2 , Q 1 , and Q 2 is an amino acid.
- Exemplary Drug Linking Assembly Units provided herein are those units that contain two Drug Units (D 1 and D 2 ) and include those represented by the following structures:
- mc-VC-PABC-D 1 is replaced with mc-VA-PABC-D 1 or mc-VA-D 1 or any other I ⁇ -D 1 unit; and/or mc-VC-PABC-D 2 is replaced with mc-VA-PABC-D 2 or mc-VA- D 2 or any other L 2 -D 2 unit; and wherein R PR is hydrogen or a protecting group, e.g., acid labile protecting group, e.g., BOC ; [0197]
- the component mc-VC-PABC-D has the structure of:
- he component mc-VA-PABC-D has the structure of:
- the component mc-VA-D has the structure of:
- mc-VC-PABC-D, mc-VA-PABC-D, mc-VA- D, and MDPr-PABC(gluc)-D are exemplary -L ⁇ D 1 or -L 2 -D 2 moieties bonded to a Drug Linking Assembly Unit (DLA) by means of Attachment Groups (Q 1 and Q 2 ), and wherein the wavy line indicates covalent bonding of the succinimide ring of mc or MDPr to a thiol present on either of Q 1 or Q 2 ;
- PABC-D wherein the mc moiety has the structure of , wherein the wavy line to the succinimide moiety indicates covalent bonding to the Drug Linking Assembly Unit (DLA) via Attachement groups Q 1 and Q 2 ), and wherein the wavy line adjacent to the carbonyl indicates covalent bonding to the remainder of -D 1 or -D 2 .
- the mc moiety may be replaced with the MDPrmoiety, which has the structure of
- MDPr-VC-PABC-D MDPr-VA-D and MDPr-VA-PABC-D, which are further exemplary -L ⁇ D 1 or -L 2 -D 2 moieties
- a Drug Linking Assembly Unit has the Formula (XHIa):
- T is a Tethering Group that can be attached to a sulfur atom of an engineered cysteine in said antibody's heavy chain or light chain or to a thiol produced by reduction of an antibody's interchain disulfide linkage;
- Q 1 is a first Attachment Group
- Q 2 is a second Attachment Group
- X B is a branched Attachment Group Linker
- D 1 is a first Drug Unit
- D 2 is a second Drug Unit
- L 1 is an Optional Linking Group joining D 1 to Q 1 ;
- L 2 is an Optional Linking Group joining D 2 to Q 2 ;
- subscripts m 1 and m 2 are each independently 0 or 1;
- Y is a Partitioning Agent that is attached to a site on L, Q 1 , X B , Q 2 , L 1 or L 2 ;
- n 0, 1, or 2.
- PEGA is a non- dispersive PEG Unit having the structure of d/or PEGB is a nondispersive PEG Unit having the structure of wherein each R 21 is an independently selected PEG capping unit, an each instance of n independently selected is an integer ranging from 8 to 24 or from 12 to 38.
- one R 21 is -CH 3 and the other is -CH 2 CH 2 C0 2 H.
- MDPr moiety which has the structure of , wherein R PR is hydrogen or a protecting group, to provide MDPr-VC-PABC-D, MDPr-VA- D and MDPr-VA-PABC-D as - V-D 1 or -L 2 -D 2 ,
- the MDPr moiety in the above structure where that moiety is present is replaced with the mc moiety to provide mc-PABC(gluc)D as -I ⁇ -D 1 or -L 2 -D 2 .
- substituted succinimide in MDPr in any one of the MDPr- containing - ⁇ ⁇ 1 or -L 2 -D 2 moieties may exist in hydrolyzed form (i.e., a water molecule is added across one and not both of the carbonyl-nitrogen bonds).
- MDPr-PABC(gluc)-D as the -I ⁇ -D 1 or -L 2 -D 2 moiety is replaced with mc-PABC(gluc)-D.
- substituted succinimide in MDPr in any one of the MDPr- containing - ⁇ ⁇ 1 or -L 2 -D 2 moieties may exist in hydrolyzed form (i.e., a water molecule is added across one and not both of the carbonyl-nitrogen bonds).
- An -I ⁇ -D 1 or -L 2 -D 2 moiety comprised of mc may also have its succinimide ring in hydrolyzed form.
- the MD-ADCs are useful for inhibiting the multiplication of a tumor cell or cancer cell, causing apoptosis in a tumor or cancer cell, or for treating cancer in a patient.
- the MD- ADCs can be used accordingly in a variety of settings for the treatment of cancers.
- the MD- ADCs can be used to deliver a drug to a tumor cell or cancer cell.
- the antibody of a MD-ADC binds to or associates with a cancer-cell or a tumor-cell-associated antigen, and the MD-ADC can be taken up (internalized) inside a tumor cell or cancer cell through receptor-mediated endocytosis or other internalization mechanism.
- the antigen can be attached to a tumor cell or cancer cell or can be an extracellular matrix protein associated with the tumor cell or cancer cell. Once inside the cell, via a cleavable mechanism, the drug is released within the cell. In an alternative embodiment, the Drug or Drug Unit is cleaved from the MD-ADC outside the tumor cell or cancer cell, and the Drug or Drug Unit subsequently penetrates the cell.
- the antibody binds to the tumor cell or cancer cell. [0208] In another embodiment, the antibody binds to a tumor cell or cancer cell antigen which is on the surface of the tumor cell or cancer cell.
- the antibody binds to a tumor cell or cancer cell antigen which is an extracellular matrix protein associated with the tumor cell or cancer cell.
- the specificity of the antibody for a particular tumor cell or cancer cell can be important for determining those tumors or cancers that are most effectively treated.
- MD-ADCs that target a cancer cell antigen present in hematopoietic cancers can be useful treating hematologic malignancies (e.g., anti-CD30, anti-CD70, anti-CD19, anti-CD33 binding antibodies can be useful for treating hematologic malignancies).
- MD-ADCs that target an accessible cancer cell antigen present on solid tumors are useful treating such solid tumors.
- Cancers treatable with a MD-ADC include, but are not limited to, hematopoietic cancers such as, for example, lymphomas (Hodgkin Lymphoma and Non-Hodgkin Lymphomas) and leukemias and solid tumors.
- hematopoietic cancers include, follicular lymphoma, anaplastic large cell lymphoma, mantle cell lymphoma, acute myeloblastic leukemia, chronic myelocytic leukemia, chronic lymphocytic leukemia, diffuse large B cell lymphoma, and multiple myeloma.
- solid tumors examples include fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma, endotheliosarcoma,
- lymphangiosarcoma lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing's tumor, leiomyosarcoma, rhabdomyosarcoma, colon cancer, colorectal cancer, kidney cancer, pancreatic cancer, bone cancer, breast cancer, ovarian cancer, prostate cancer, esophageal cancer, stomach cancer, oral cancer, nasal cancer, throat cancer, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinomas, cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, seminoma, embryonal carcinoma, Wilms' tumor, cervical cancer, uterine cancer, testicular cancer, small cell lung carcinoma, bladder carcinoma, lung cancer, epithelial carcinoma, gli
- Cancers including, but not limited to, a tumor, metastasis, or other disease or disorder characterized by uncontrolled cell growth, can be treated or inhibited by administration of a MD- ADC.
- methods for treating cancer including
- chemotherapeutic agent In one embodiment the chemotherapeutic agent is that with which treatment of the cancer has not been found to be refractory. In another embodiment, the chemotherapeutic agent is that with which the treatment of cancer has been found to be refractory. In some embodiments, an MD-ADC is administered to a patient that has also undergone surgery as treatment for the cancer.
- the patient also receives an additional treatment, such as radiation therapy.
- an additional treatment such as radiation therapy.
- the MD-ADC is administered concurrently with the chemotherapeutic agent or with radiation therapy.
- the chemotherapeutic agent or radiation therapy is administered prior or subsequent to
- the chemotherapeutic agent is administered over a series of sessions.
- Those embodiments include administration of any one or a combination of the chemotherapeutic agents, such a standard of care chemotherapeutic agent(s).
- methods of treatment of cancer with a MD-ADC are provided as an alternative to chemotherapy or radiation therapy where the chemotherapy or the radiation therapy has proven or can prove too toxic, e.g., results in unacceptable or unbearable side effects, for the subject being treated.
- the patient being treated is optionally treated with another cancer treatment such as surgery, radiation therapy or chemotherapy, depending on which treatment is found to be acceptable or bearable.
- the MD-ADCs are useful for killing or inhibiting the replication of a cell that produces an autoimmune disease or for treating an autoimmune disease.
- the MD-ADCs can be used accordingly in a variety of settings for the treatment of an autoimmune disease in a patient.
- the MD-ADCs can be used to deliver a drug to a target cell.
- the MD-ADC associates with an antigen on the surface of a target cell, and the MD-ADC is then taken up inside a target-cell through receptor-mediated endocytosis. Once inside the cell, the Linker unit is cleaved, resulting in release of the Drug or Drug Unit.
- the released Drug is then free to migrate in the cytosol and induce cytotoxic or cytostatic activities.
- the Drug is cleaved from the MD-ADC outside the target cell, and the Drug or Drug Unit subsequently penetrates the cell.
- the antibody binds to an autoimmune antigen.
- the antigen is on the surface of a cell involved in an autoimmune condition.
- the antibody binds to an autoimmune antigen which is on the surface of a cell. [0220] In one embodiment, the antibody binds to activated lymphocytes that are associated with the autoimmune disease state.
- the MD-ADC kills or inhibit the multiplication of cells that produce an autoimmune antibody associated with a particular autoimmune disease.
- Th2 lymphocyte related disorders e.g., atopic dermatitis, atopic asthma, rhinoconjunctivitis, allergic rhinitis, Omenn's syndrome, systemic sclerosis, and graft versus host disease
- Thl lymphocyte-related disorders e.g., rheumatoid arthritis, multiple sclerosis, psoriasis, Sjorgren's syndrome, Hashimoto's thyroiditis, Grave's disease, primary biliary cirrhosis, Wegener's granulomatosis, and tuberculosis
- activated B lymphocyte-related disorders e.g., systemic lupus erythematosus, Goodpasture's syndrome, rheumatoid arthritis, and type I diabetes.
- Methods for treating an autoimmune disease including administering to a patient in need thereof an effective amount of a MD-ADC and another therapeutic agent known for the treatment of an autoimmune disease.
- compositions and Methods of Administration [0224]
- the present invention provides pharmaceutical compositions comprising the MD- ADCs described herein and a pharmaceutically acceptable carrier.
- the MD-ADCs are in any form that allows for the Conjugate to be administered to a patient for treatment of a disorder associated with expression of the antigen to which the antibody binds.
- the Conjugate is administered to a patient for treatment of a disorder associated with expression of the antigen to which the antibody binds.
- Conjugates are preferably in the form of a liquid or solid.
- the preferred route of administration is parenteral.
- Parenteral administration includes subcutaneous injections, intravenous, intramuscular, intrasternal injection or infusion techniques.
- the preferred route of administration is parenteral.
- Parenteral administration includes subcutaneous injections, intravenous, intramuscular, intrasternal injection or infusion techniques.
- the preferred route of administration is parenteral.
- Parenteral administration includes subcutaneous injections, intravenous, intramuscular, intrasternal injection or infusion techniques.
- the preferred route of administration is parenteral.
- Parenteral administration includes subcutaneous injections, intravenous, intramuscular, intrasternal injection or infusion techniques.
- compositions are administered parenterally.
- the conjugates are administered intravenously.
- Administration is conducted by any convenient route, for example by infusion or bolus injection.
- Pharmaceutical compositions are formulated so as to allow a compound to be bioavailable upon administration of the composition to a patient.
- Compositions will take the form of one or more dosage units, where for example, a tablet can be a single dosage unit.
- compositions are non-toxic in the amounts used. It will be evident to those of ordinary skill in the art that the optimal dosage of the active ingredient(s) in the pharmaceutical composition will depend on a variety of factors. Relevant factors include, without limitation, the type of animal (e.g., human), the particular form of the compound, the manner of administration, and the composition employed.
- composition in some embodiments, is in the form of a liquid, preferably ones useful for delivery by injection.
- a surfactant preferably ones useful for delivery by injection.
- one or more of a surfactant, preservative, wetting agent, dispersing agent, suspending agent, buffer, stabilizer and isotonic agent is optionally present.
- the liquid compositions include one or more of the following: sterile diluents such as water for injection, saline solution, preferably physiological saline, Ringer's solution, isotonic sodium chloride, fixed oils such as synthetic mono or digylcerides which can serve as the solvent or suspending medium, polyethylene glycols, glycerin, cyclodextrin, propylene glycol or other solvents; antibacterial agents such as benzyl alcohol or methyl paraben; antioxidants such as ascorbic acid or sodium bisulfite; chelating agents such as ethylenediaminetetraacetic acid; buffers such as amino acids, acetates, citrates or phosphates; detergents, such as nonionic surfactants, polyols; and agents for the adjustment of tonicity such as sodium chloride or dextrose.
- sterile diluents such as water for injection, saline solution, preferably physiological saline, Ringer's solution, is
- a parenteral composition is preferably enclosed in ampoule, a disposable syringe or a multiple-dose vial made of glass, plastic or other material.
- Physiological saline is an exemplary adjuvant.
- An injectable composition is preferably sterile.
- the amount of the conjugate that is effective in the treatment of a particular disorder or condition will depend on the nature of the disorder or condition, and can be determined by standard clinical techniques. In addition, in vitro or in vivo assays are optionally employed to help identify optimal dosage ranges. The precise dose to be employed in the compositions will also depend on the route of administration, and the seriousness of the disease or disorder, and should be decided according to the judgment of the practitioner and each patient's circumstances.
- compositions comprise an effective amount of a compound such that a suitable dosage will be obtained. Typically, this amount is at least about 0.01% of a compound by weight of the composition.
- the composition preferably comprise from about 0.01 to about 100 mg of a MD-ADC per kg of the animal's body weight. In one embodiment, the composition includes from about 1 ⁇ g to about 100 mg of a MD-ADC per kg of the animal's body weight. In other embodiments, the amount administered will be in the range from about 0.1 to about 25 mg/kg of body weight of a compound.
- the dosage of a conjugate administered to a patient is typically about 0.01 mg/kg to about 100 mg/kg of the subject's body weight. In some embodiments, the dosage administered to a patient is between about 0.01 mg/kg to about 15 mg/kg of the subject's body weight. In some embodiments, the dosage administered to a patient is between about 0.1 mg/kg and about 15 mg/kg of the subject's body weight. In some embodiments, the dosage
- the administered to a patient is between about 0.1 mg/kg and about 20 mg/kg of the subject's body weight. In some embodiments, the dosage administered is between about 0.1 mg/kg to about 5 mg/kg or about 0.1 mg/kg to about 10 mg/kg of the subject's body weight. In some
- the dosage administered is between about 1 mg/kg to about 15 mg/kg of the subject's body weight. In some embodiments, the dosage administered is between about 1 mg/kg to about 10 mg/kg of the subject's body weight. In some embodiments, the dosage administered is between about 0.1 to 4 mg/kg, even more preferably 0.1 to 3.2 mg/kg, or even more preferably 0.1 to 2.7 mg/kg of the subject's body weight over a treatment cycle.
- carrier refers to a diluent, adjuvant or excipient, with which a compound is administered.
- Such pharmaceutical carriers include liquids, such as water and oils, including those of petroleum, animal, vegetable or synthetic origin, such as peanut oil, soybean oil, mineral oil, sesame oil.
- Other carriers include saline, gum acacia, gelatin, starch paste, talc, keratin, colloidal silica, urea.
- auxiliary, stabilizing, thickening, lubricating and coloring agents are optionally used.
- the compound or compositions and pharmaceutically acceptable carriers are sterile. Water is an exemplary carrier when the compounds are administered intravenously.
- Saline solutions and aqueous dextrose and glycerol solutions are preferably employed as liquid carriers, particularly for injectable solutions.
- Suitable pharmaceutical carriers also include excipients such as starch, glucose, lactose, sucrose, gelatin, malt, rice, flour, chalk, silica gel, sodium stearate, glycerol monostearate, talc, sodium chloride, dried skim milk, glycerol, propylene, glycol, water, and ethanol.
- the present compositions if desired, can also contain minor amounts of wetting or emulsifying agents, or pH buffering agents.
- the conjugates are formulated in accordance with routine procedures as a pharmaceutical composition adapted for intravenous administration to animals, particularly human beings.
- the carriers or vehicles for intravenous administration are sterile isotonic aqueous buffer solutions.
- the compositions can also include a solubilizing agent.
- Compositions for intravenous administration optionally comprise a local anesthetic such as lignocaine to ease pain at the site of the injection.
- the ingredients are supplied either separately or mixed together in unit dosage form, for example, as a dry lyophilized powder or water free concentrate in a hermetically sealed container such as an ampoule or sachette indicating the quantity of active agent.
- a conjugate is to be administered by infusion, it is dispensed, for example, with an infusion bottle containing sterile pharmaceutical grade water or saline. Where the conjugate is administered by injection, an ampoule of sterile water for injection or saline is provided so that the ingredients can be mixed prior to administration.
- the pharmaceutical compositions are generally formulated as sterile, substantially isotonic and in full compliance with all Good Manufacturing Practice (GMP) regulations of the U.S. Food and Drug Administration.
- GMP Good Manufacturing Practice
- the present disclosure provides antibody-drug conjugate (ADC) linkers that are Orthogonally' protected (i.e. protected to allow for selective deprotection when the attachment of a Drug Units is being carried out.
- Orthogonally protected antibody drug conjugated linkers are characterized as linking assembly (LA) units that include Protecting Groups on each Attachment Group (e.g. Q 1 and Q 2 ).
- LA linking assembly
- Attachment Groups allow for the covalent attachment of the Drug Units; however, the Protecting Groups of the present disclosure block the covalent attachment of a Drug moiety to the linking assembly and are removable under specific conditions.
- Orthogonally protected Linking Assembly Unit are designed to incorporate different Protecting Groups allowing for selective deprotection and addition of a chosen Drug Unit.
- orthogonally protected Linking Assembly Unit [0237] In certain embodiments, orthogonally protected Linking Assembly Unit
- T is a Tethering Group which facilitates attachment to the antibody thiols produced by reduction of the antibody's interchain disulfide linkages
- Q 1 is a first Attachment Group that allows for covalent attachment of a first Drug Unit (D 1 );
- Q 2 is a second Attachment Group that allows for covalent attachment of a second Drug Unit
- P 1 is a first Protecting Group blocking the covalent attachment of first Drug Unit (D 1 );
- P 2 is a second Protecting Group blocking the covalent attachment of first Drug Unit (D 1 ), and P 1 and P 2 are different;
- X is an Attachment Group Linker that provides a connection between two Attachment Groups
- Y is a Partitioning Agent
- n 0 or 1.
- orthogonally protected Linking Assembly Unit are characterized by the structure of Formula (lib):
- T is a Tethering Group which facilitates attachment to the antibody thiols produced by reduction of the antibody's interchain disulfide linkages
- each Q 1 is a first Attachment Group that allows for covalent attachment of a first Drug Unit (D 1 );
- Q 2 is a second Attachment Group that allows for covalent attachment of a second Drug Unit
- P 1 is a first Protecting Group blocking the covalent attachment of first Drug Unit (D 1 );
- P 2 is a second Protecting Group blocking the covalent attachment of first Drug Unit (D 1 ), and P 1 and P 2 are different;
- X is an Attachment Group Linker
- Y is a partitioning group
- n 0 or 1.
- orthogonally protected Linking Assembly Unit are characterized by the Formula (Illb)
- T is a Tethering Group which facilitates attachment to the antibody thiols produced by reduction of the antibody's interchain disulfide linkages
- each Q 1 is an independently selected a first Attachment Group that allow for covalent attachment of an independently selected first Drug Unit (D 1 );
- Q 2 is a second Attachment Group that allows for covalent attachment of a second Drug Unit
- P 1 is a first Protecting Group blocking the covalent attachment of first Drug Unit (D 1 );
- P 2 is a second Protecting Group blocking the covalent attachment of first Drug Unit (D 1 ), and P 1 and P 2 are different;
- X 1 and X 2 are each an Attachment Group Linker;
- Y is a partitioning group
- n 0 or 1.
- orthogonally protected Linking Assembly Unit are characterized by the Formula (IVb)
- T is a Tethering Group having a terminal maleimido moiety
- Q 1 is a first Attachment Group comprising a first cysteine moiety or an analogue thereof;
- Q 2 is a second Attachment Group comprising a second cysteine moiety or an analogue thereof;
- X 1 and X 2 are each an Attachment Group Linker;
- P 1 is a first thiol Protecting Group
- P 2 is a second thiol Protecting Group, and P 1 and P 2 are different;
- Y is a Partitioning Agent attached to L, Q 1 , X or Q 2 ;
- n 0 or 1.
- the Tethering Group (T), Attachment Groups (Q 1 and Q 2 , Attachment Group Linkers (X, X 1 , and X 2 ), optional Partitioning Agents (Y) are as defined in the preceding Linking Assembly Unit section.
- a Drug Unit may be added to the selectively deprotected linker.
- Drug Units may include Optional Linking Groups L 1 and L 2 .
- T is a Tethering Group having a terminal maleimido moiety.
- Q 1 is a first Attachment Group comprising a first cysteine moiety or an analogue thereof;
- Q 2 is a second Attachment Group comprising a second cysteine moiety or an analogue thereof;
- P 1 is a first thiol Protecting Group; and
- P 2 is a second thiol Protecting Group, and P 1 and P 2 are different.
- 'Orthogonal' deprotection (i.e. selective deprotection) of a Linker Assembly Unit having suitable protection allows for the synthesis of Drug Linker Assembly Units with a specifically desired ratio of D 1 to D 2 Drug Units and a mechanism to uniformly delivery this desired ratio of drugs to a target site.
- Protecting Groups (P 1 and P 2 ) are selectively removable units which can attach to Attachment units (Q 1 and Q 2 ). In order for 'Orthogonal' deprotection, the identity of P 1 and P 2 are different.
- P 1 and P 2 are thiol Protecting Groups.
- P 1 is selected from the group consisting of -S-isopropyl (SiPr), -S-tert-butyl (StBu), and -S-methyl (SMe); and P 2 is -CH 2 NH-C(0)CH 3 (acetamidomethyl).
- the orthogonally protected Linking Assembly Unit is represented by Formulas lb, lib, Illb, or IVb, and T is MDPr-Val-Cit-; P 1 is selected from the group consisting of -S-isopropyl (SiPr), -S-tert-butyl (StBu), and -S-methyl (SMe); and P 2 is - CH 2 NH-C(0)CH 3 (acetamidomethyl).
- the orthogonally protected Linking Assembly Unit is represented by Formulas lb, lib, Illb, or IVb, and X is selected from the group consisting of glycine and alanine; T is MDPr-Val-Cit-; P 1 is selected from the group consisting of -S- isopropyl (SiPr), -S-tert-butyl (StBu), and -S-methyl (SMe); and P 2 is -CH 2 NH-C(0)CH 3 (acetamidomethyl).
- the orthogonally protected Linking Assembly Unit is represented by Formulas lb, lib, Illb, or IVb, and T is MDPr-Val-Cit-; Q 1 and Q 2 are each cysteine; X is glycine; P 1 is selected from the group consisting of -S-isopropyl (SiPr), -S-tert- butyl (StBu), and -S-methyl (SMe); and P 2 is -CH 2 NH-C(0)CH 3 (acetamidomethyl).
- the orthogonally protected Linking Assembly Unit is represented by Formulas lb, lib, Illb, or IVb, and T is MDPr-Val-Cit-; Q 1 and Q 2 are each cysteine; X is glycine; P 1 is selected from the group consisting of -S-isopropyl (SiPr), -S-tert- butyl (StBu), and -S-methyl (SMe); P 2 is -CH 2 NH-C(0)CH 3 (acetamidomethyl); the subscript n is 1 and Y comprises a PEG or cyclodextrin group.
- Preparative reverse-phase FEPLC was performed on a Varian ProStar 210 solvent delivery system configured with a Varian ProStar 330 PDA detector. Products were purified over a Phenomenex Synergy MAX-RP 30.0 x 250 mm, 4 um, 80 A reverse phase column eluting with 0.05 % trifluoroacetic acid in water (solvent A) and 0.0.5 % trifluoroacetic acid in acetonitrile (solvent B).
- the purification methods generally consisted of linear gradients of solvent A to solvent B, ramping from 90% aqueous solvent A to 10% solvent A. The flow rate was 5.0 mL/min with monitoring at 220 nm.
- Resin loading In a 10 mL solid phase reaction vessel (plastic syringe with PET frit) was added 0.15 g of 2-Cl-Tritylchloride resin (0.225 mmol) followed by a solution of Fmoc- amino acid or Fmoc-amino-PEG 24 -COOH (0.225 mmol, 1.0 equiv) and N,N- diisopropylethylamine (DIPEA) (0.338 mmol, 1.5 equiv) in 3 mL of dry CH 2 C1 2 . The vessel was shaken for 5 min, then more DIPEA (0.225 mmol, 1.0 equiv) was added, and the vessel was shaken for additional 30 min.
- DIPEA N,N- diisopropylethylamine
- Fmoc removal procedure Resin containing Fmoc-protected peptide was treated with 20 % piperidine in DMF (5 x 3 mL) for 30 min total. The resin was then washed with DMF (5 x 5 mL) prior to further manipulation.
- Fmoc-Cys amino acids (1 equiv) were coupled by adding a solution containing Fmoc-Cys (4 equiv), hydroxybenzotriazole (HOBT) (4 equiv), and ⁇ , ⁇ '-diisopropylcarbodiimide (DIC) (4 equiv).
- HOBT hydroxybenzotriazole
- DIC ⁇ , ⁇ '-diisopropylcarbodiimide
- Samples were reduced with 10 mM dithiothreitol (DTT) for 10 min at 37 °C and then chromatographed over an analytical reversed-phase column (Agilent Technologies, PLRP-S, 30 ⁇ , 2.1 mm ID x 50 mm, 3 ⁇ ) at 80°C and eluted with a linear gradient of 0.01% TFA in acetonitrile from 25% to 65% in 0.05% aqueous TFA over 5 minutes, followed by isocratic 65% 0.01% TFA in acetonitrile for 0.5 min at a flow rate of 1.0 mL/min.
- DTT dithiothreitol
- Mass spectrometry data was acquired in ESI+ mode using a mass range of 500-4000 m/z and were deconvoluted using MaxEntl to determine masses of the resulting conjugates.
- the extent of aggregation of the conjugates was determined by size-exclusion chromatography (SEC) using an analytical SEC column (Sepax SRT-C 300 7.8 mm ID x 30 cm, 5 ⁇ ) on a Waters 2695 FEPLC system.
- the injected material was eluted using an isocratic mixture of 92.5% 25 mM sodium phosphate (pH 6.8), 350 mM NaCl, and 7.5% isopropyl alcohol at a flow rate of 1 mL/min.
- ADCs were prepared by reduction of antibody interchain disulfides followed by addition of a 25-100%» excess maleimide as described previously.
- Full reduction of 8 thiols per antibody was accomplished by addition of 12 equivalents of tris(2-carboxyethyl)-phosphine (TCEP) to an antibody solution (1-10 mg/mL in PBS, pH 7.4). The extent of antibody reduction was monitored by reverse-phase LC-MS and additional TCEP was added as needed to complete the reaction. TCEP was then removed by ultrafiltration (3x, 10-fold dilution into PBS, pH 7.4 containing 1 mM EDTA, centrifugation at 4000 x g through a 30-kDa MWCO filter).
- NEM N-ethylmaleimide
- Example 3 General procedure for dual-modified antibody conjugates.
- Carrier 4 conjugation To fully reduced cACIO antibody in PBS-EDTA was added 16 equiv. of carrier 4 from a 10 mM DMSO stock. The resulting solution was vortexed and left at room temperature for 15 min. At this time, reverse-phase LC-MS indicated full alkylation of antibody thiols with no loss of fidelity of the Acm protecting group. The conjugate was purified by ultrafiltration according to the procedures described above.
- the resulting solution was vortexed and left at room temperature for 15 min. At this time, reverse-phase LC-MS was used to judge reaction progress, and additional drug-linker or NEM was added as needed until all thiols had been alkylated.
- the conjugate was purified by gel filtration or ultrafiltration according to the procedures described above.
- Second conjugation To a solution containing cAClO-4-drug/NEM with 8 free thiols was added 50-100% molar excess of maleimide drug-linker or NEM from a 10 mM DMSO stock. The resulting solution was vortexed and left at room temperature for 15 min. At this time, reverse-phase LC-MS was used to judge reaction progress, and additional drug-linker or NEM was added as needed until all thiols had been alkylated. The conjugate was purified by gel filtration or ultrafiltration according to the procedures described above. [0268] The average drugs per antibody during each step of the conjugation process was within 2.5% of complete drug loading (8 drugs/mAb), as determined by reverse-phase HPLC.
- Example 4 Cell binding analysis [0280] Binding of antibody or ADC to cell-surface CD30 was assessed by flow cytometry on CD30(+) L540cy Hodgkin lymphoma cells. Cells (2 x 10 5 ) were combined with 4-fold serial dilutions of each antibody treatment in flow buffer (PBS, 2 % fetal bovine serum, 0.2 % NaN 3 ) in a total volume of 100 ⁇ . The cells were incubated on ice for 30 min, and then washed twice with ice-cold flow buffer.
- PBS 2 % fetal bovine serum
- a FITC-labeled goat anti-human Fc secondary antibody (109-095-098, Jackson ImmunoResearch) was added at the recommended dilution in a total volume of 100 ⁇ ⁇ flow buffer.
- the cells were incubated on ice for 30 min, and then washed twice with ice-cold flow buffer. Labeled cells were examined by flow cytometry on an Attune NxT flow cytometer (Thermo Fisher Scientific). Data was analyzed using Flow Jo software and plotted using GraphPad Prism 6. Binding constants were determined by nonlinear regression using a one site binding model. Results are shown in FIG.8.
- L540cy Hodgkin lymphoma
- DEL DEL-BVR [6] (anaplastic large cell lymphomas)
- U-266 multiple myeloma
- L540cy and DEL were obtained from DSMZ
- U-266 was obtained from ATCC.
- Authenticity of cell lines was confirmed using the Cell Check 16 panel (IDEXX Bioresearch).
- U- 266 cells stably expressing firefly luciferase were generated using in vivo ready lentiviral particles from GenTarget, Inc. (San Diego, CA).
- U-266 cells were grown to 1 x 10 6 cells/mL (>90% viable) and transduced with lentiviral particles for 72 hours in RPMI 1640 media + 10% FBS. Cells were placed under selection in neomycin and stable clones were produced by dilution cloning into 96 well plates. A stable U-2661uc cell line was selected using the Bright-Glo Luciferase Assay System (Promega) using an En Vision Multilabel Plate Reader (Perkin Elmer). For all cytotoxicity experiments, cells were cultured in log-phase growth, then seeded for 24 hours in 96-well plates containing 150 uL RPMI-1640 supplemented with 10-20 % FBS.
- Example 6 Comparison of co-administration of 2 ADCs versus co-conjugation of 2 drugs on 1 ADC
- ADCs were added to cells at the same total antibody concentration and cytotoxicity was measured as outlined above. Competition for receptor binding leads to decreased activity (on an antibody basis) for co-administration. On cell lines with low receptor copy number, the effect can be more pronounced.
- mice were randomized to study groups when the average tumor volume reached approximately 100 mm 3 .
- Example 8 Dual ADCs compared to 8- and/or 16-load single drug ADCs
- ADCs having either mcMMAF (Comp. Aa) or mc-vc-MMAE (Comp. Ab) were compared to a dual-auristatin ADC bearing Comp. Aa/Comp. Ab at matched drug loads of 16 drugs per antibody.
- the co-conjugate having Comp. Aa and Comp Ab
- Aa (16) (a single-drug 16-load ADC with only Comp. Aa as the drug unit). This was despite the hBU12-Linking Assembly Unit Aa (8)-Comp.
- ADC a single-drug 16-load ADC with only Comp.
- a dual- auristatin ADC targeting LIV-1 with the hLIV22 antibody had significantly higher in vitro activity compared to either single-drug 16-load ADC. This data demonstrates that the co- conjugated auristatin ADCs demonstrate improved cytotoxic activity independent of antibody or cell line.
- co-conjugated ADCs with auristatin drugs are broadly active
- the tables below show that co-conjugated ADCs delivering other payloads can have high activity.
- camptothectin, dolastatin, and vinblastine can be incorporated into co-conjugated ADCs to provide enhanced activity.
- Linking Assembly Unit Aa referred to above as drug carrier 4: Linking Assembly Unit Aa comprises MDPr, PEG24, 1 SiPr, and 1 Acm protected Cys residue.
- Chronic exposure assay 10 million cells were plated in a T225 flask in the appropriate cell media. ADC was added at a concentration of 100 ng/mL. Media was replaced every four days containing fresh ADC. After 15 days, the cells were washed with PBS, fixed with 3.7 % paraformaldehyde, and then stained with a 0.5% solution of crystal violet. The number of remaining cell colonies (>5 cells) was then counted. Results for h25G5 ADCs:
- Example 10 Drug carrier bearing 3 cysteines for 16 + 8 drug loading:
- Example 11 A PEG arm is not requir r dual-conjugates bearing hydrophilic drugs.
- Example 12 In vitro cytotoxicity of dual-auristatin ADCs on L49 antibody targeting MFI2 (p97)
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Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111565752A (en) * | 2017-11-18 | 2020-08-21 | 恩佐拉·德马加尔海斯 | Products and methods using GC7 (N1-carbamimidoyl-1, 7-diaminoheptane) based antigen binding conjugates in tumor therapy |
US20190343828A1 (en) * | 2018-04-06 | 2019-11-14 | Seattle Genetics, Inc. | Camptothecin peptide conjugates |
TW202015740A (en) * | 2018-06-07 | 2020-05-01 | 美商西雅圖遺傳學公司 | Camptothecin conjugates |
CN111378006A (en) * | 2018-12-28 | 2020-07-07 | 联宁(苏州)生物制药有限公司 | Novel double-arm intermediate LND1026-035 for antibody coupling drug and synthetic method thereof |
JP7232925B2 (en) * | 2019-02-15 | 2023-03-03 | ウーシー バイオロジクス アイルランド リミテッド | Process for preparing antibody drug conjugates with improved homogeneity |
WO2021022678A1 (en) | 2019-08-07 | 2021-02-11 | 烟台迈百瑞国际生物医药股份有限公司 | Antibody-drug conjugate and application thereof |
US20230097908A1 (en) * | 2020-01-22 | 2023-03-30 | Medimmune Limited | Compounds and conjugates thereof |
CN116390770A (en) * | 2020-05-13 | 2023-07-04 | 思进股份有限公司 | Methods of treating cancer using combinations of anti-CD 30 antibody-drug conjugates |
CN111560078A (en) * | 2020-06-19 | 2020-08-21 | 联宁(苏州)生物制药有限公司 | Double-arm intermediate with maleimide joint and synthetic method thereof |
CN113941007A (en) * | 2020-07-16 | 2022-01-18 | 成都科岭源医药技术有限公司 | Serial-connection double-medicine link assembly unit and application thereof |
CN114053426A (en) * | 2020-07-30 | 2022-02-18 | 成都科岭源医药技术有限公司 | Double-drug linked assembly unit and double-drug targeting joint-drug conjugate |
CN115105607A (en) * | 2021-03-22 | 2022-09-27 | 成都科岭源医药技术有限公司 | Preparation method and application of double-drug-linker for ADC (analog to digital converter) |
CN117177775A (en) * | 2021-04-14 | 2023-12-05 | 启德医药科技(苏州)有限公司 | Linker, conjugate and uses thereof |
WO2022268050A1 (en) * | 2021-06-22 | 2022-12-29 | 荣昌生物制药(烟台)股份有限公司 | Pharmaceutical combination and use thereof |
US20230270874A1 (en) * | 2021-07-19 | 2023-08-31 | Mabplex International Co., Ltd. | Antibody drug conjugate loaded with binary toxins and its application |
CA3230737A1 (en) | 2021-09-03 | 2023-03-09 | Toray Industries, Inc. | Pharmaceutical composition for cancer treatment and/or prevention |
US11814394B2 (en) * | 2021-11-16 | 2023-11-14 | Genequantum Healthcare (Suzhou) Co., Ltd. | Exatecan derivatives, linker-payloads, and conjugates and thereof |
WO2023198884A1 (en) * | 2022-04-14 | 2023-10-19 | Debiopharm Research & Manufacturing S.A. | Ligand-drug-conjugates with improved pharmacokinetic and drug release properties |
WO2023225359A1 (en) * | 2022-05-20 | 2023-11-23 | Novartis Ag | Antibody-drug conjugates of antineoplastic compounds and methods of use thereof |
WO2023223097A1 (en) * | 2022-05-20 | 2023-11-23 | Novartis Ag | Antibody drug conjugates |
WO2024002154A1 (en) * | 2022-06-28 | 2024-01-04 | Genequantum Healthcare (Suzhou) Co., Ltd. | Anti-fgfr3 antibody conjugate and medical use thereof |
WO2024012569A1 (en) * | 2022-07-15 | 2024-01-18 | Genequantum Healthcare (Suzhou) Co., Ltd. | Linkers, conjugates and applications thereof |
Family Cites Families (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8308235D0 (en) | 1983-03-25 | 1983-05-05 | Celltech Ltd | Polypeptides |
GB8422238D0 (en) | 1984-09-03 | 1984-10-10 | Neuberger M S | Chimeric proteins |
AU606320B2 (en) | 1985-11-01 | 1991-02-07 | International Genetic Engineering, Inc. | Modular assembly of antibody genes, antibodies prepared thereby and use |
US5225539A (en) | 1986-03-27 | 1993-07-06 | Medical Research Council | Recombinant altered antibodies and methods of making altered antibodies |
DE68925966T2 (en) | 1988-12-22 | 1996-08-29 | Kirin Amgen Inc | CHEMICALLY MODIFIED GRANULOCYTE COLONY EXCITING FACTOR |
US5530101A (en) | 1988-12-28 | 1996-06-25 | Protein Design Labs, Inc. | Humanized immunoglobulins |
US5166322A (en) | 1989-04-21 | 1992-11-24 | Genetics Institute | Cysteine added variants of interleukin-3 and chemical modifications thereof |
JP2763020B2 (en) | 1995-04-27 | 1998-06-11 | 日本電気株式会社 | Semiconductor package and semiconductor device |
US5672662A (en) | 1995-07-07 | 1997-09-30 | Shearwater Polymers, Inc. | Poly(ethylene glycol) and related polymers monosubstituted with propionic or butanoic acids and functional derivatives thereof for biotechnical applications |
CA2262994A1 (en) | 1996-08-02 | 1998-02-12 | Ortho-Mcneil Pharmaceutical, Inc. | Polypeptides having a single covalently bound n-terminal water-soluble polymer |
EP1545613B9 (en) | 2002-07-31 | 2012-01-25 | Seattle Genetics, Inc. | Auristatin conjugates and their use for treating cancer, an autoimmune disease or an infectious disease |
WO2006113909A2 (en) | 2005-04-19 | 2006-10-26 | Seattle Genetics, Inc. | Humanized anti-cd70 binding agents and uses thereof |
US8088387B2 (en) | 2003-10-10 | 2012-01-03 | Immunogen Inc. | Method of targeting specific cell populations using cell-binding agent maytansinoid conjugates linked via a non-cleavable linker, said conjugates, and methods of making said conjugates |
KR101520209B1 (en) | 2003-11-06 | 2015-05-13 | 시애틀 지네틱스, 인크. | Monomethylvaline compounds capable of conjugation to ligands |
EP1747021B1 (en) | 2004-05-19 | 2015-09-09 | E. R. Squibb & Sons, L.L.C. | Self-immolative linkers and drug conjugates |
US20060292616A1 (en) | 2005-06-23 | 2006-12-28 | U.S. Genomics, Inc. | Single molecule miRNA-based disease diagnostic methods |
AU2006269940C1 (en) | 2005-07-18 | 2013-11-07 | Seagen Inc. | Beta-glucuronide-linker drug conjugates |
SI1813614T1 (en) | 2006-01-25 | 2012-01-31 | Sanofi 174 | Cytotoxic agents comprising new tomaymycin derivatives |
WO2008025020A2 (en) | 2006-08-25 | 2008-02-28 | Seattle Genetics, Inc. | Cd30 binding agents and uses thereof |
CA2683568A1 (en) * | 2007-05-08 | 2008-11-20 | Genentech, Inc. | Cysteine engineered anti-muc16 antibodies and antibody drug conjugates |
HUE031533T2 (en) | 2007-10-19 | 2017-07-28 | Seattle Genetics Inc | Cd19 binding agents and uses thereof |
DK2644194T3 (en) | 2008-03-18 | 2017-07-03 | Genentech Inc | Combinations of an anti-HER2 antibody-drug conjugate and docetaxel |
EP3360879A1 (en) | 2009-02-05 | 2018-08-15 | ImmunoGen, Inc. | Benzodiazepine derivatives as cytotoxic agents |
FR2949469A1 (en) | 2009-08-25 | 2011-03-04 | Sanofi Aventis | ANTICANCER DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION |
US9849192B2 (en) | 2009-11-18 | 2017-12-26 | Rutgers, The State University Of New Jersey | Targeting tumor cells with chemotherapeutic agents conjugated to matriptase antibodies |
KR101738203B1 (en) | 2010-04-15 | 2017-05-19 | 메디뮨 리미티드 | Pyrrolobenzodiazepines and conjugates thereof |
CA3220104A1 (en) | 2010-06-08 | 2011-12-15 | Genentech, Inc. | Cysteine engineered antibodies and conjugates |
MX346635B (en) | 2011-02-15 | 2017-03-27 | Immunogen Inc | Cytotoxic benzodiazepine derivatives. |
KR102084806B1 (en) | 2012-02-17 | 2020-03-04 | 시애틀 지네틱스, 인크. | ANTIBODIES TO INTEGRIN αvβ6 AND USE OF SAME TO TREAT CANCER |
KR102433686B1 (en) | 2012-05-15 | 2022-08-19 | 씨젠 인크. | Self-stabilizing linker conjugates |
US9504756B2 (en) | 2012-05-15 | 2016-11-29 | Seattle Genetics, Inc. | Self-stabilizing linker conjugates |
AU2014337317A1 (en) | 2013-10-15 | 2016-09-15 | Sorrento Therapeutics Inc. | Drug-conjugates with a targeting molecule and two different drugs |
US11103593B2 (en) | 2013-10-15 | 2021-08-31 | Seagen Inc. | Pegylated drug-linkers for improved ligand-drug conjugate pharmacokinetics |
KR102462811B1 (en) | 2015-04-27 | 2022-11-04 | 에이비온 주식회사 | Dendron conjugated antibody and use thereof |
WO2016190770A1 (en) | 2015-05-22 | 2016-12-01 | Общество С Ограниченной Ответственностью "Отечественные Фармацевтические Технологии" | Novel derivatives of 3,5-divinyl-pyrazole for medical application |
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